Site Activation Manager With Expertise In Clinical Trials
hace 5 días
**About the Role**
We are seeking a highly skilled Site Activation Manager to join our team at Syneos Health, a leading biopharmaceutical solutions organization. This is an excellent opportunity for a dedicated professional to contribute to the success of our customers and help bring life-changing treatments to market.
**Responsibilities**
The successful candidate will be responsible for ensuring quality deliverables at the country level, following project requirements and applicable country rules with moderate oversight from the SSU Country Manager. They will work within forecasted submission/approval timelines and ensure compliance with these deadlines, tracking progress in real-time using the agreed-upon SSU tracking system.
If forecasted timelines are not met, the Site Activation Manager will investigate the reasons for delays, provide clear rationale, support contingency planning to mitigate impact, and escalate issues as necessary.
In addition, they will monitor basic financial aspects of projects and contracts, escalating discrepancies in a timely fashion. The Site Activation Manager will also review and comply with Standard Operating Procedures (SOPs) and Work Instructions (WI), keeping training records up-to-date and ensuring timesheet compliance.
The ideal candidate will have a detailed understanding of clinical trial processes across Phases II-IV and ICH GCP, as well as excellent communication and problem-solving skills.
**What We Offer**
We offer a competitive salary range of $65,000 - $85,000 per annum, depending on experience, as well as a comprehensive benefits package, including health insurance, retirement plan, and paid time off.
Our team at Syneos Health values diversity, inclusion, and employee development, and we strive to create a positive work environment that fosters growth and collaboration. If you are passionate about the healthcare industry and possess strong organizational skills, we encourage you to apply for this exciting opportunity.
-
Clinical Research Manager
hace 4 semanas
Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completoJob SummaryMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Clinical Research Manager to lead our global clinical trials efforts. As a key member of our team, you will be responsible for managing clinical trials from feasibility to close-out, ensuring compliance with regulatory requirements and company standards.Key...
-
Clinical Trials Operations Coordinator
hace 6 días
Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completoCompany Overview:Worldwide Clinical Trials (WCT) is a leading global contract research organization that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications.The company has a dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, which...
-
Clinical Operations Specialist for Clinical Trials
hace 2 horas
Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completoWe are seeking a highly organized and detail-oriented Clinical Operations Specialist to join our team at Worldwide Clinical Trials.About the Role:The Clinical Operations Specialist will be responsible for ensuring all daily aspects of operational work related to rater selection, certification/qualification, training content, scale acquisition, surveillance...
-
Ciudad de México, Ciudad de México ICON Plc A tiempo completoRegulatory Affairs Specialist with Expertise in Clinical TrialsAt ICON Plc, we're seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs team, you will be responsible for leading the preparation, submission, and maintenance of regulatory documents for clinical trials. Your expertise in clinical...
-
Regulatory Affairs Specialist
hace 1 mes
Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo**About the Role**We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Worldwide Clinical Trials. As a key member of our team, you will be responsible for planning, initiating, and tracking documents required for regulatory submissions, essential documents collection, review, and provision of country/site/EC requirements to...
-
Strategic Clinical Trials Director
hace 2 semanas
Ciudad de México, Ciudad de México Eli Lilly and Company A tiempo completoJob DescriptionLeverage your expertise in clinical trials and site engagement to drive success at Eli Lilly and Company. As a Strategic Clinical Trials Director - Site Engagement, you will be responsible for leading a team of Clinical Research Leads within the country and collaborating with business partners to execute clinical trials/studies across all...
-
Regulatory Affairs Specialist
hace 4 semanas
Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo**Role Overview**At Worldwide Clinical Trials, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. This role will be responsible for planning, initiating and tracking documents required for regulatory submissions, essential documents collection, review and provision of country/site/EC requirements to support achievement of site...
-
Clinical Trial Site Activation Specialist
hace 1 mes
Ciudad de México, Ciudad de México PSI A tiempo completoJob DescriptionAt PSI, we are seeking a highly skilled Clinical Trial Site Activation Specialist to join our team. As a key member of our project teams, you will play a critical role in ensuring the smooth and timely activation of clinical trial sites in Mexico.Key ResponsibilitiesOversee and coordinate the processes critical for clinical trial sites...
-
Clinical Trials Project Manager
hace 1 semana
Ciudad de México, Ciudad de México IQVIA A tiempo completoJob OverviewWe are seeking an experienced Clinical Trials Project Manager to lead and oversee the execution of clinical projects and research studies in accordance with global and local regulations.Key Responsibilities:Support in ensuring compliance with contract, SOPs, GCPs, policies, and regulatory requirements.Meeting quality & timeline metrics.Effective...
-
Clinical Trials Specialist
hace 7 días
Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completoJob OverviewMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Regulatory Specialist to play a key role in the success of our clinical trials. As a Regulatory Specialist, you will be responsible for ensuring compliance with regulatory requirements and guidelines, coordinating with investigative sites, and maintaining awareness...
-
Clinical Trials Specialist
hace 1 mes
Ecatepec de Morelos, México Syneos Health Clinical A tiempo completoAbout the RoleSyneos Health Clinical is seeking a highly skilled Clinical Trials Specialist to join our team. As a Clinical Trials Specialist, you will be responsible for ensuring the smooth conduct of clinical trials, from site qualification to close-out visits. You will work closely with project teams to ensure regulatory compliance and provide guidance to...
-
Global Clinical Trials Manager
hace 3 días
Ciudad de México, Ciudad de México Eli Lilly and Company A tiempo completoJob OverviewWe are seeking a highly skilled Global Clinical Trials Manager to join our team at Eli Lilly and Company.About the RoleThe successful candidate will lead and manage a team of clinical research professionals within the country, collaborating with business partners to ensure clinical trials/studies across all therapeutic areas are executed in...
-
Clinical Research Specialist
hace 1 mes
Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completoAbout the RoleWe are seeking a skilled Clinical Research Specialist to join our team at Worldwide Clinical Trials. As a Clinical Research Specialist, you will be responsible for all aspects of assigned projects, including clinical assessment, training development, and data review.Key ResponsibilitiesAssist in the review of eCOA/ePRO specifications and engage...
-
Ciudad de México, Ciudad de México ICON Plc A tiempo completoRegulatory Affairs Specialist RoleAt ICON Plc, we're seeking a skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs department, you will be responsible for leading the preparation, submission, and maintenance of regulatory documents for clinical trials.Key Responsibilities:Prepare and submit regulatory documents...
-
Clinical Research Manager
hace 1 mes
Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completoAbout the RoleMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly motivated and experienced Clinical Research Manager to join our team. As a key member of our clinical operations team, you will be responsible for managing clinical trials from feasibility to close-out, ensuring timely and efficient execution of studies.Key...
-
Clinical Assessment Specialist
hace 7 días
Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completoWorldwide Clinical Trials (Worldwide) is a leading global contract research organization that works in partnership with biotechnology and pharmaceutical companies to create customized solutions for advancing new medications.We are seeking a highly skilled Clinical Assessment Specialist to join our team. As a key member of the Clinical Assessment Technologies...
-
Ciudad de México, Ciudad de México IQVIA A tiempo completoWe are seeking a skilled Senior Regulatory Specialist to join our team at IQVIA. This individual will be responsible for site activation and regulatory affairs in Mexico.Estimated Salary Range: $60,000 - $90,000 per yearJob Description:Company Overview: As a leading global provider of advanced analytics, technology solutions, and clinical research services...
-
Clinical Trials Senior Analyst
hace 4 semanas
Ciudad de México, Ciudad de México Novo Nordisk AS A tiempo completoAre you passionate about clinical trials and ensuring compliance with Mexican importation and exportation laws? We are looking for a Clinical Trials Senior Analyst to join our team at Novo Nordisk A/S in Mexico. If that sounds like you, read on to learn more about this exciting opportunity.The PositionAs a Clinical Trials Senior Analyst, you will be...
-
Clinical Trials Risk Manager
hace 2 semanas
Ciudad de México, Ciudad de México SAO Fortrea Brazil Limitada A tiempo completoSAO Fortrea Brazil Limitada is seeking a highly skilled Clinical Trials Risk Manager to join their team.About the RoleThis is a critical position that requires a deep understanding of clinical trials and risk management. As a Clinical Trials Risk Manager, you will be responsible for ensuring the full implementation of the risk plan and recommending...
-
Clinical Trials Specialist
hace 4 días
Ecatepec de Morelos, México Syneos Health Clinical A tiempo completoAbout the Role:As a Clinical Trials Specialist at Syneos Health Clinical, you will play a crucial role in ensuring the success of our clinical trials. Your primary responsibility will be to conduct site qualification, initiation, monitoring calls, and close-out visits for remote sites.Responsibilities:Conduct site qualification, initiation, monitoring calls,...