Equal opportunity and affirmative action employer (us applicants only) straumann group is an equal opportunity employer and will not discriminate against any employee or applicant for employment on the basis of race, color, sex, sexual orientation, gender identity, religion, creed, national origin, age, veteran status, or disability unrelated to job requirements. straumann group will take affirmative action to ensure that qualified applicants are employed and that employees are treated without regard to their race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran and disability status. in compliance with u.s. department of labor executive order 11246, section 503 of the rehabilitation act, and section 4212 of the vietnam era readjustment assistance act, straumann group has developed and maintains an affirmative action program and plan. we comply with the employee polygraph protection act (eppa), and massachusetts law. it is unlawful for private employers to use lie detector tests for pre-employment screening or during employment, except in limited circumstances. an employer who violates this law shall be subject to criminal penalties and civil liability. . get tailored job recommendations based on your interests. profile icon ${profiledata.firstname ? profiledata.firstname.substring(0,1) : ''} ${profiledata.firstname.substring(0,1)} hi ${profiledata.firstname ? profiledata.firstname : 'user'}, you've got a ${widgetbundle[fit.name] | pht : jobjobmatchsdata[eachjob['jobseqno']][fit.name].data} match score for this job...
Equal opportunity and affirmative action employer (us applicants only) straumann group is an equal opportunity employer and will not discriminate against any employee or applicant for employment on the basis of race, color, sex, sexual orientation, gender identity, religion, creed, national origin, age, veteran status, or disability unrelated to job requirements. straumann group will take affirmative action to ensure that qualified applicants are employed and that employees are treated without regard to their race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran and disability status. in compliance with u.s. department of labor executive order 11246, section 503 of the rehabilitation act, and section 4212 of the vietnam era readjustment assistance act, straumann group has developed and maintains an affirmative action program and plan. we comply with the employee polygraph protection act (eppa), and massachusetts law. it is unlawful for private employers to use lie detector tests for pre-employment screening or during employment, except in limited circumstances. an employer who violates this law shall be subject to criminal penalties and civil liability. . get tailored job recommendations based on your interests. profile icon ${profiledata.firstname ? profiledata.firstname.substring(0,1) : ''} ${profiledata.firstname.substring(0,1)} hi ${profiledata.firstname ? profiledata.firstname : 'user'}, you've got a ${widgetbundle[fit.name] | pht : jobjobmatchsdata[eachjob['jobseqno']][fit.name].data} match score for this job...
Elevate your career with the hart team! are you ready to launch your career to new heights in an inspiring, forward-thinking environment? at the hart team, we’re not just looking to fill a role; we’re inviting a transaction coordinator to become a core part of our success story! if you’re ambitious, strategic, and eager to make a real impact in the world of real estate, this is your moment. in this role, you’ll work directly with our executive team, sparking innovation and helping shape our vision. here, your creativity is celebrated, your growth is prioritized, and every contribution you make is valued. ready to make waves in real estate? let’s connect! join our team and make an impact! we handle and close more than 100 transactions each year, keeping up a fast-paced momentum that fuels our team’s drive and success! we're a proudly part of exp realty, the top cloud-based real estate brokerage known for innovation, excellence, and expansive market reach. led by wayne hartard, an icon agent ranking in the top 3% out of over 90,000 agents at exp realty, we bring unparalleled expertise and dedication to every client and transaction. the role you will be responsible for : oversee a pipeline of 150+ active transaction files, ensuring each file progresses smoothly from start to close. track deadlines, required documentation, and client communications for each transaction, proactively managing any potential delays. responsible for opening all transaction files and creating new listings for properties as they come on the market. build detailed property listings, ensuring accuracy a...
Equal opportunity and affirmative action employer (us applicants only) straumann group is an equal opportunity employer and will not discriminate against any employee or applicant for employment on the basis of race, color, sex, sexual orientation, gender identity, religion, creed, national origin, age, veteran status, or disability unrelated to job requirements. straumann group will take affirmative action to ensure that qualified applicants are employed and that employees are treated without regard to their race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran and disability status. in compliance with u.s. department of labor executive order 11246, section 503 of the rehabilitation act, and section 4212 of the vietnam era readjustment assistance act, straumann group has developed and maintains an affirmative action program and plan. we comply with the employee polygraph protection act (eppa), and massachusetts law. it is unlawful for private employers to use lie detector tests for pre-employment screening or during employment, except in limited circumstances. an employer who violates this law shall be subject to criminal penalties and civil liability. . get tailored job recommendations based on your interests. profile icon ${profiledata.firstname ? profiledata.firstname.substring(0,1) : ''} ${profiledata.firstname.substring(0,1)} hi ${profiledata.firstname ? profiledata.firstname : 'user'}, you've got a ${widgetbundle[fit.name] | pht : jobjobmatchsdata[eachjob['jobseqno']][fit.name].data} match score for this job...
About bad marketing: we're a team of 170+ passionate leaders and creatives who have worked diligently to make bad marketing one of the largest and most robust growth marketing agencies in the world. at the core of our philosophy is the belief that excellence stems from a united team working toward a common objective: to not only help our clients grow profitably but also to provide them with an experience they can’t find anywhere else. we specialize in local lead generation, e-commerce, and information marketing; catering to clients that span from auto and local shop owners, to online consumer product brand owners, online gurus selling courses or coaching, and more. our approach to success involves more than just b old a nd d isruptive strategies. we invest in our team through extensive training, continuous support for growth and learning, and the cultivation of a happy and confident company culture. for us, finding fulfillment in your career is just as crucial as excelling in it. about this position: as an email & sms designer, you will play an important role in creating captivating email and sms campaigns, delivering visual messaging and optimize email designs for optimal ctr and conversions. you will be responsible for staying on brand with each client by using the correct fonts, colors, and visuals provided by each client’s branding guidelines. responsibilities: create compelling and high converting graphic designs for email marketing campaigns. design and design and develop email templates including icon/ui creation and gifs. a/b test your designs. daily use of k...
Pharmacovigilance reporting associate icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development we are currently seeking a pharmacovigilance reporting associate to join our diverse and dynamic team. as a pharmacovigilance reporting associate at icon, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities. you will ensure compliance with regulatory requirements and contribute to the effective management of safety data to support patient safety and regulatory compliance. what you will be doing: preparing and reviewing safety reports, including periodic safety updates and individual case safety reports, ensuring accuracy and compliance with regulatory standards. collecting and analyzing adverse event data from clinical trials and post-marketing sources to support the preparation of comprehensive safety reports. maintaining up-to-date knowledge of regulatory requirements and industry best practices related to pharmacovigilance reporting. collaborating with cross-functional teams, including clinical, regulatory, and data management, to gather necessary information and resolve any reporting issues. ensuring the timely submission of safety reports to regulatory authorities and sponsors, adhering to established deadlines and guidelines. your profile: bachelor’s degree in life sciences, pharmacy, or a r...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, alzheimer’s and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes. verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. participates in audit preparation and follow-up activities as needed. may serve as preceptor, providing training to less experienced clinical team members. you are: bachelor’s degree in a health, life sciences or other relevant field of study. previous experience supporting clinical trials including 4 years of experience on site monitoring tasks. pr...
Home based icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. we are currently seeking a pharmacovigilance associate to join our diverse and dynamic team. as a pharmacovigilance associate at icon, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance. what you will be doing: collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. conducting signal detection and risk assessment activities to identify potential safety issues. collaborating with cross-functional teams to support safety-related inquiries and investigations. maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. assisting in the preparation of safety reports and regulatory submissions. your profile: bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred. experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment. strong analytical skills with attention to detail in data collection and reporting. excellent communication and interper...
Tienes wifi y sabes utilizar tu computador, entonces puedes ganar dinero desde casa. el marketing digital es una opción real para trabajar desde casa y ganar dinero . si en este momento te sientes identificado con una de las siguientes situaciones: [wps_lists icon=»arrow-right» icon_color=»#81d742″] tienes más de 40 años y no consigues empleo? tienes un grupo de amigos y contactos, y te gustaría poder venderles algún producto pero no sabes cuál? tienes una idea de negocio y no sabes por donde comenzar? quieres promocionar tu propia idea de negocio y no sabes como hacerlo? te gustaría comercializar productos de china en redes sociales? quieres vender tus productos durante la temporada de fin de año? quieres vender productos digitales sin tener productos propios? te interesa el tema pero consideras que hay un exceso de información y no sabes por donde comenzar? quieres prepararte en marketing digital como opción complementaria de formación? quieres tener una fuente de ingreso complementaria o principal? te gustaría poder recibir un acompañamiento en marketing digital en el que puedas hacer todas las preguntas que tengas? [/wps_lists] cierre de inscripciones: 30 de noviembre si la respuesta a alguna de las preguntas anteriores es si, te invito a ver el siguiente video:...
Project manager/sr project manager, feasibility site activation - homebased - mexico, brazil, colombia, chile and peru icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development role summary: accountable for driving and accelerating the activation of global investigative sites in line with, or ahead of, the study's contractual timelines, within budgeted resources, with quality output, and exceeding sponsor expectations. accountable for the overall coordination, implementation and completion of site activation or maintenance activities for assigned projects of work in line with icon/sponsor sops as appropriate, including regulatory/ethics, site contracts, essential documents, and site activations. interacts with internal teams and stakeholders, as well as sponsor teams and stakeholders as needed. you will be doing: lead studies with highest quality standards to exceed customer expectations. review study and partnership budgets for proposals and sales as needed. drive assigned studies to meet kpis and delight customers and sites act as customer point of contact for assigned studies; resolve study issues and drive exceptional customer delivery represent fsa at audits and inspections participate in business development opportunities to support the growth of the assigned portfolio, function, and/or region/country(ies) travel (approximately 10% depending on country structure and dire...
As clinical research associate (cra), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes. - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. ...
Icon plc is a world-leading healthcare intelligence and clinical research organization. from molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. with our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. our people are our greatest strength, are at the core of our culture, and the driving force behind our success. icon people have a mission to succeed and a passion that ensures what we do, we do well. we have an incredible opportunity for a **principal clinical data science lead** to join icon. **locations**: - mexico (office-based with remote flexibility) - colombia (office-based or home-based) **overview of the role**: this principal clinical data science lead (cdsl) role is part of the early phase data management department and is responsible for managing data management teams, studies, and programs of studies under the general direction of the senior manager/director of data management. the principal cdsl will provide planning estimates for project scope, schedule, and resource requirements, and ensures that studies are properly managed and delivered. they will work with clinical operations, biostatistics, sas programming, medical writing, and quality assurance to ensure that data collected during trials is managed according to corporate standards and meets regulatory guidelines for data integrity. the early phase service line of the co...
Icon plc is a world-leading healthcare intelligence and clinical research organization. from molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. with our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. our people are our greatest strength, are at the core of our culture, and the driving force behind our success. icon people have a mission to succeed and a passion that ensures what we do, we do well. we have an incredible opportunity for a **clinical data lead** to join the team. **location**: - mexico (home based - colombia (home based) **overview of the role**: as a clinical data lead (cdl) you will be the point of contact for day to day activity on a study with key responsibilities for study set-up and close-out tasks as well as overseeing and coordinating tasks delegated to the study team members both locally and in other offices. you will also coordinate with data management teams, studies and programs of studies and independently oversee the performance of data management activities on multiple studies. - independently prepare all materials and take part in study kick off (internal and external) meeting. - review all activity on an ongoing basis to identify out of scope tasks and bring to the attention of the dmpm and contract analyst. - lead the development of specifications, implementation, and testing for the ecrf or paper crf. ...
Empresa de hoteleria, hostal y entretenimiento icon suites, necesita un equipo de trabajo de obreros de construccion para finalizar un proyecto pausado. objetivo: preparar terrenos de **construcción**, cavar zanjas, colocar refuerzos en las paredes laterales de las excavaciones, construir andamios y limpiar escombros, restos, y otros materiales de desecho. pueden ayudar a trabajadores en otros oficios de la **construcción**. **requisitos**: contar con su estricto equipo de trabajo de soluciones con respecto a lo indicado. horario: lunes a viernes de 9:00 am a 5:00 pm tipo de puesto: tiempo completo...
As a graduate pharmacovigilance associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. working in this program you will feel challenged and supported to advance in your professional career while making a truly impact. **what you will be doing**: - perform processing for all types of safety events, reconciliation of saes, literature surveillance, data retrievals from the safety database, medical information call handling activities and other medically related project information under mentorship of a drug safety associate or above. - ensure all icon, sponsor, and regulatory timeframes are met for the processing and reporting of safety information - assist in ensuring the completion of all departmental project activities accurately in accordance with icon standards, regulatory requirements, and contractual obligations to sponsors for icon strategic solutions, may also include: - serve as safety reporting processor for assigned projects, providing support as designated. - complete adverse event and/or product quality complaint cases follow up in writing and/or by phone based on requirements for each client. - supports periodic reconciliation of adverse event and/or quality complaint cases received from different sources within the required deadlines - serve as quality complaint processor for assigned projects and monitor the process of retu...
Job title: pharmacovigilance associate job location: bogotá, bogota, colombia job location type: on-site job contract type: permanent job seniority level: home based icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. we are currently seeking a pharmacovigilance associate to join our diverse and dynamic team. as a pharmacovigilance associate at icon, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance. what you will be doing: collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. conducting signal detection and risk assessment activities to identify potential safety issues. collaborating with cross-functional teams to support safety-related inquiries and investigations. maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. assisting in the preparation of safety reports and regulatory submissions. your profile: bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred. experience in pharmacovigilance, drug safety, or a related area, preferably within a clini...
Icon plc is a world-leading healthcare intelligence and clinical research organization. from molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. with our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. our people are our greatest strength, are at the core of our culture, and the driving force behind our success. icon people have a mission to succeed and a passion that ensures what we do, we do well. we have an incredible opportunity for a **clinical data lead** to join the team. **location**: - mexico (home based - colombia (home based) **overview of the role**: as a clinical data lead (cdl) you will be the point of contact for day to day activity on a study with key responsibilities for study set-up and close-out tasks as well as overseeing and coordinating tasks delegated to the study team members both locally and in other offices. you will also coordinate with data management teams, studies and programs of studies and independently oversee the performance of data management activities on multiple studies. - independently prepare all materials and take part in study kick off (internal and external) meeting. - review all activity on an ongoing basis to identify out of scope tasks and bring to the attention of the dmpm and contract analyst. - lead the development of specifications, implementation, and testing for the ecrf or paper crf. ...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. - may ...
As clinical research associate (cra), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. -...
As a senior regulatory affairs specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. the senior regulatory affairs associate has responsibility for providing comprehensive regulatory services to clients within the pharmaceutical, biologic, medical device or other regulatory services environments. this will include support for assessment, registration, maintenance and other activities as assigned. you will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. working in this program you will feel challenged and supported to advance in your professional career while making a truly impact. **what you will be doing**: the regulatory affairs specialist will be working with drugs' registration according to the local regulatory agencies. - perform all electronic submissions of registration and post-registration requests to regulatory agencies. - ensure all expected/required correct data is updated/ uploaded in the systems (veeva) - supports assigned teams in the preparation of all submission types in adherence with applicable legislation, regulations and guidelines facilitating approvals and continued client compliance. - maintains a positive and productive liaison with internal and external contacts. this may include clients, regulatory agencies, and related institutions. - assists in the development of assessments and strategic regulatory plans for client product development programs. supports the develo...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. - may be assigned clinical tasks where advanced negotiating skills are required. **you are**: - bachelor’s degree in a health, life sciences or other relevant field of study. ...
Management assistant - colombia, bogota hybrid: office/remote icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development management assistant office based role (hybrid) - mexico city, mexico - bogotá, colombia icon plc is a world-leading healthcare intelligence and clinical research organisation. from molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. with our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. our people are our greatest strength, are at the core of our culture, and the driving force behind our success. icon people have a mission to succeed and a passion that ensures what we do, we do well. the role: as a management assistant at icon, your job is essential in latam regional support across all divisions (ibt, ipd, iod, idc), supporting the regional leadership governance meetings and actions, capabilities & country input for sales/pm/feasibility/ssu, etc. this is a role that responds to the special requirement and needs for the region to have a governance and oversight that helps the global services be able to receive information on latam and respond to growth in the region for clinical operations this support includes quality...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. - may be assigned clinical tasks where advanced negotiating skills are required. **you are**: - bachelor’s degree in a health, life sciences or other relevant field of study. ...
Unleash your potential with us! are you ready to take your career to new heights in a vibrant, forward-thinking environment? at the hart team, we’re not just offering a job; we’re inviting you to be a key player in our dynamic team! we’re on the lookout for an executive assistant / operations manager who is not afraid to think big and challenge the norm. in this exciting role, you’ll partner directly with our ceo and executive team, driving innovation and shaping our organizational vision. if you have a passion for real estate, a knack for strategic thinking, and a desire to make an impactful difference, this is your chance to shine! join us and become part of a culture where your creativity is celebrated, your ideas are valued, and your contributions propel us forward. are you ready to make waves? let’s connect! join our team and make an impact! we handle and close more than 100 transactions each year, keeping up a fast-paced momentum that fuels our team’s drive and success! we're a proudly part of exp realty, the top cloud-based real estate brokerage known for innovation, excellence, and expansive market reach. led by wayne hartard, an icon agent ranking in the top 3% out of over 90,000 agents at exp realty, we bring unparalleled expertise and dedication to every client and transaction. the role we are looking for a proactive and innovative executive assistant / operations manager to support our ceo and executive team. this role is more than just calendar management; we need a strategic partner who can think creatively, manage staff effectively, and align with the organiz...
Elevate your career with the hart team! are you ready to launch your career to new heights in an inspiring, forward-thinking environment? at the hart team, we’re not just looking to fill a role; we’re inviting a transaction coordinator to become a core part of our success story! if you’re ambitious, strategic, and eager to make a real impact in the world of real estate, this is your moment. in this role, you’ll work directly with our executive team, sparking innovation and helping shape our vision. here, your creativity is celebrated, your growth is prioritized, and every contribution you make is valued. ready to make waves in real estate? let’s connect! join our team and make an impact! we handle and close more than 100 transactions each year, keeping up a fast-paced momentum that fuels our team’s drive and success! we're a proudly part of exp realty, the top cloud-based real estate brokerage known for innovation, excellence, and expansive market reach. led by wayne hartard, an icon agent ranking in the top 3% out of over 90,000 agents at exp realty, we bring unparalleled expertise and dedication to every client and transaction. the role you will be responsible for : be the voice of success: strong verbal and written communication skills that engage and inspire. daily client prospecting: generate new clients every day from a variety of lead sources! respond rapidly: handle all inbound leads from internet sources, sign calls, and beyond. coordinate key appointments: set up appointments for our listing and buyer specialists. master lead management: input, organize and manage...
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