Why This Role Matters Are you ready to take your monitoring expertise to the next level and mentor the next generation of clinical research professionals? As a Senior Clinical Research Associate I (SCRA I), you will oversee
Support an employee experience that is compliant, accurate, and well-managed. As a Benefits Administration Analyst, you will administer benefit programs, partner with vendors, and respond to employee inquiries with professionalism. You’ll help maintain disciplined controls and
About MEDLIFE: MEDLIFE is a global nonprofit organization that empowers students to become leaders in service while improving access to healthcare, education, and safe housing in underserved communities around the world. We are looking for energetic,
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind
Position Summary: The Business Development Associate is responsible for end-to-end pipeline development and opportunity intelligence within the clinical research lifecycle. This role focuses exclusively on identifying, evaluating, qualifying, and advancing clinical trial opportunities aligned with organizational capabilities
Bristol Myers Squibb is seeking a Clinical Research Associate to serve as the primary site contact, ensuring quality, integrity and compliance of clinical trial activities in line with protocol, SOPs, ICH GCP and regulatory requirements. This role
Position Summary The Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance of clinical trial sites in accordance
Associate Site Activation Manager Summary: The Associate Global Site Activation Manager (SAM) in the GSL team at IQVIA serves as the project manager for the start‑up phase, leading the design and implementation of the site activation strategy from
Job Overview Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams. Perform, manage and co-ordinate activities for assigned opportunities/ projects. Perform data mining and analysis, formulate recommendations
Parexels Functional Service Provider (FSP) is looking for CRAs II, SR CRAs I and II to join our team in Argentina, Brazil or Mexico. The Clinical Research Associate II will be responsible for data integrity, data quality
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine: IQVIA Biotech is a full-service CRO purpose-built to
When our values align, theres no limit to what we can achieve. Parexel FSP is hiring multipleSite Care Partners inArgentina (Buenos Aires)! Excellent opportunity for experienced Senior CRAs with +5 years of experience, ready to take
Parexel FSP is hiring multiple Site Care Partners in Argentina (Buenos Aires)! Excellent opportunity for experienced Senior CRAs with +5 years of experience, ready to take the next step in their career! The Site Care Partner
_IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine:_ _IQVIA Biotech is a full-service CRO purpose-built to
Job Overview Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams. Perform, manage and co-ordinate activities for assigned opportunities/ projects. Perform data mining and analysis, formulate recommendations