Senior Clinical Research Associate

Parexel Senior Clinical Research Associate-FSP Role SummaryAt Parexel, we're committed to delivering excellence in clinical research and development. As a Senior Clinical Research Associate-FSP, you'll play a key role in ensuring the success of our clients' clinical trials. Your expertise in site management will be instrumental in building strong...

Unlock a fulfilling career with Parexel as a Clinical Research Associate Senior, where you will utilize your expertise to drive site management success. With a strong background in clinical research and a proven track record of delivering results, you will be responsible for ensuring the integrity of study implementation at assigned sites.About the RoleThis...

About the RoleParexel is seeking an experienced Senior Clinical Research Associate to join our team. As a Senior Clinical Research Associate, you will be responsible for managing clinical trials from site identification to close-out.Key ResponsibilitiesSite Management: Act as Parexel's direct point of contact with assigned sites, assess and ensure overall...

Job Title:Senior Clinical Research Associate - Field Support Partner

Job SummaryAs a Senior Clinical Research Associate-FSP at Parexel, you will be responsible for ensuring the overall integrity of study implementation and adherence to study protocol at clinical sites. You will act as Parexel's direct point of contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study...

About the JobParexel is seeking a skilled Clinical Research Associate to join our team in [location]. This role will involve working with clients to ensure the successful execution of clinical trials, providing expert guidance on site management and ensuring compliance with regulatory requirements.Key ResponsibilitiesAct as Parexel's direct point of contact...

Job SummaryWe are seeking a highly skilled and experienced Clinical Research Associate-FSP Manager to join our team at Parexel. As a key member of our site management team, you will be responsible for overseeing the day-to-day activities of clinical research sites, ensuring compliance with regulatory requirements and study protocols.About UsParexel is a...

Job Summary:Parexel is seeking a highly skilled Clinical Research Associate-FSP to join our team. As a Clinical Research Associate-FSP, you will be responsible for ensuring the overall integrity of study implementation and adherence to study protocol at clinical sites.Key Responsibilities:Act as Parexel's direct point of contact with assigned sites,...

About the RoleParexel is seeking a highly skilled Clinical Research Associate to join our team as a Study Management Professional.Job DescriptionAs a Clinical Research Associate, you will be responsible for ensuring the timely and accurate completion of project goals and updating applicable trial management systems. Your primary focus will be on site...

Job OverviewAs a Clinical Research Assistant Intern at IQVIA, you will provide administrative and technical support to our team. Your primary responsibility will be to assist our Clinical Research Associates (CRAs) and Clinical Trial Assistants (CTAs) in their daily work.Qualifications• Bachelor's degree in a relevant field (e.g., medicine, life...

**Job Overview**: Provide administrative and technical support to our team.**Responsibilities**: Assist Clinical Research Associates and Assistants with daily tasks.**Qualifications**:Bachelor's Degree in a relevant field.Strong communication and problem-solving skills.Ability to work effectively in a team environment.**About IQVIA**: We are a leading...

Company OverviewIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.Job DescriptionProvides administrative and/or...

Parexel is seeking a skilled Clinical Trial Manager to join our team.About the RoleThis is a critical position that requires strong problem-solving skills, ability to work independently, and excellent communication skills. The successful candidate will be responsible for ensuring timely and accurate completion of project goals and update of applicable trial...

At Parexel, We're Committed to Delivering Exceptional ResultsAbout UsParexel is a global biopharmaceutical outsourcing company that provides a broad range of solutions, from clinical trials to commercialization. Our mission is to support our clients in bringing new treatments to patients worldwide. When our values align, there's no limit to what we can...

Parexel's Commitment to ExcellenceThe Site Contract Associate plays a pivotal role in ensuring the success of our clinical trials by negotiating and finalizing site contracts that meet the highest standards of quality and compliance.Key Responsibilities:Negotiate and finalize site contracts, ensuring alignment with regulatory requirements and company...

Key Responsibilities:The Site Contract Associate ('SCA') is responsible for negotiation, finalization, and execution of all types of site contracts required for site activation. This includes ancillary documents associated with site contracts. Post site activation, the SCA is responsible for negotiation, finalization, and execution of any amendments to the...

A Career Defining OpportunityCerence Inc., a global leader in creating cutting-edge AI-powered solutions, is seeking an exceptional Principal Research Developer, LLM to join our team. As a key member of our research team, you will be responsible for architecting, designing, and implementing state-of-the-art generative AI models for dialog, destination entry,...

Unlock Your Potential in Contract ManagementThe Site Contract Associate plays a pivotal role in our team, responsible for negotiating and finalizing site contracts. This key position ensures the highest standard of quality in documents, adhering to regulatory requirements and company guidelines. By fostering positive relationships with clinical trial sites,...

Clinical Education and Support RoleAt CN20 Alcon (China) Ophthalmic Product Co. Ltd Company, we are seeking a skilled Ophthalmic Development Professional to join our team.About the RoleThis position involves providing field support to customers and other personnel, as well as conducting on-site education and consulting to establish and maintain relationships...

Role OverviewWe're seeking a Senior Data Architect to join our EPAM China Data & Analytics Team.As a senior member of the team, you'll contribute to constructing top-tier data solutions and applications vital for organizational decision-making.Key responsibilities include:Designing and implementing MLOps platforms on AzureResearching and evaluating platform...