Clinical Research QA & Monitoring Lead
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A healthcare organization is seeking a Clinical Research Program Manager to oversee quality assurance for clinical trials. The candidate will ensure compliance with regulatory standards and manage ongoing monitoring activities. Required qualifications include a Bachelor's degree, 5 years of experience, and strong project management skills. This role demands leadership and the ability to work independently. Competitive compensation and benefits offered. #J-18808-Ljbffr
$71.9k - $189k
...IQVIA Argentina is seeking a Clinical Research Associate for Gloucester, NJ. The successful candidate will perform site monitoring visits and collaborate with study teams. Essential qualifications include a Bachelor's Degree and at least 2 years of on-site monitoring experience...Suggested$115k - $125k
...A leading clinical research organization is seeking a Clinical Research Associate (CRA) for a remote permanent position based out of CST. The CRA will conduct site monitoring visits, support subject recruitment, and manage communication with study sites. Candidates should...SuggestedPermanent employmentRemote work- ...Precision Medicine Group is seeking a Senior Clinical Research Associate. You will monitor clinical studies, coordinate activities, and mentor junior staff. The ideal candidate has a university degree in life sciences or health-related fields and at least 3.5 years of...SuggestedRemote workWork from home
- ...AstraZeneca GmbH is seeking a Clinical Research Associate located in New York or New Jersey to ensure timely delivery of studies at assigned sites. The CRA will collaborate closely with Local Study Teams, manage site responsibilities, and ensure compliance with regulatory...SuggestedLocal area
$79.72k - $119.58k
...Description The Senior Clinical Research Monitor is responsible for performing ongoing internal reviews of research projects where human subject research is involved to ensure investigators are compliant with federal regulations and guidelines governing clinical research...SuggestedTraineeshipRemote work- ...A leading organization in clinical research is seeking a Clinical Research Associate to ensure that clinical studies are conducted in compliance with... ...regulatory requirements. The role involves significant travel, monitoring clinical sites, and maintaining robust documentation...Remote work
- ...ICON is looking for a Clinical Research Associate in St. Louis who will play an essential role in clinical trials, ensuring protocol compliance... ...or healthcare-related field and at least 9 months of monitoring experience are essential. ICON values inclusion and offers competitive...
$91.5k - $137.3k
...A clinical research organization is seeking a Clinical Research Associate II to oversee study site management in a remote capacity. Ideal candidates will have a degree in a scientific discipline and at least two years of CRA experience, especially in oncology trials. The...Remote work$40.55 - $47.2 per hour
...Weill Cornell Medical College is seeking a Clinical Research Monitor responsible for overseeing investigator compliance with institutional requirements. This role includes planning and conducting quality audits and providing compliance training. Candidates must hold a...Hourly payMonday to Friday$40.55 - $47.2 per hour
...Title: Clinical Research Monitor Location: Upper East Side Org Unit: Genetic Medicine Work Days: Monday-Friday Weekly Hours: 35.00 Exemption Status: Non-Exempt Salary Range: $40.55 - $47.20 *As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role...Work experience placementLocal areaImmediate startMonday to Friday- ...IQVIA in New York is seeking a Clinical Research Associate (CRA) to join our team dedicated to advancing clinical research and improving patient outcomes. In this role, you'll lead site monitoring, ensure compliance with GCP/ICH guidelines, and collaborate with cross-functional...
- ...Parexel International is seeking a Senior Clinical Research Associate (SrCRA) for local responsibilities in study delivery. The role involves monitoring clinical study sites, ensuring compliance with regulations, and collaborating closely with the study team. The ideal...Local areaRemote work
- Syneos Health/ inVentiv Health Commercial LLC in Oklahoma is seeking a Clinical Research Associate to perform site qualifications, management activities, and ensure compliance with ICH-GCP guidelines. The successful candidate will maintain communication with site personnel...Flexible hours
- ...Job Title: Director Medical Monitor, Location: Parsippany, NJ, Type: Direct Hire, Contractor... ...Provide medical oversight for assigned clinical studies from study start-up through... ...preferred. Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable...For contractorsLocal area
- Syneos Health/ inVentiv Health Commercial LLC is hiring a Clinical Research Associate responsible for performing site qualification and ensuring compliance with regulatory standards. This role will involve site management activities both on-site and remotely, as well as...Remote workFlexible hours
$60 - $70 per hour
...Job Description Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating... ...Role We are seeking a Part-Time Psychedelic Dosing Monitor / Therapist to support clinical trials focused on psychedelic...Hourly payPart timeRemote work3 days per week$240k - $275k
...Senior Director, Medical Monitor, Hematology-Oncology Location... ...NY (Hybrid) Department: Clinical Development - Clinical Sciences... ...will guide clinical strategy, lead medical oversight for... ...pharma/biotech, academic clinical research, or equivalent environment....$70.1k - $126.1k
...Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate who will be responsible for site qualification, monitoring, and ensuring compliance with regulatory standards. The role involves close collaboration with various stakeholders...- ...A leading clinical research organization is seeking a CRA II to manage study sites and ensure compliance with protocols. Responsibilities include... ...patient safety, conducting site visits, and preparing monitoring reports. The ideal candidate will have a minimum of two years...Night shift
- ...A leading clinical research organization in New York is looking for a Clinical Research Associate to provide support for clinical trials. The... ...with protocol design, site evaluations, and ongoing study monitoring. Candidates should have a BA, BS, RN, BSN or equivalent, along...
$70.1k - $126.1k
...Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to join their Clinical Solutions team, responsible for monitoring trial sites to ensure compliance with regulations. Key responsibilities include site qualification and close-out activities, performed...Remote work- ...Medical Device company, has engaged GForce Life Sciences to source a skilled Clinical Site Lead (CSL). The CSL will oversee clinical study site maintenance, data collection, and field monitoring to ensure compliance with protocols, regulations, and Good Clinical...Local areaRemote workWork from home
- ...Syneos Health is seeking a Clinical Research Associate (CRA) in Austria. In this role, you will manage site qualifications, ensuring compliance... ...will possess a Bachelor’s degree or RN and previous monitoring experience in Austria, along with fluency in both German and...
- ...ProTrials Research, Inc. is seeking a Contract Senior Clinical Research Associate to oversee clinical trial monitoring and management. This role involves ensuring compliance with protocols and SOPs while managing site personnel training and documentation. The ideal candidate...Contract work
- ...PSI CRO is hiring a Medical Monitor (US Board-Certified Oncologist) to provide medical input on clinical studies remotely from the US. The ideal candidate holds a Medical... ...experience in both clinical practice and research. You will collaborate with various stakeholders...Remote work
- ...seeking a CRA/Sr. CRA to ensure quality in clinical trial management and compliance. The successful candidate will oversee monitoring activities, safeguard patient rights, and... ...demands extensive experience in clinical research, proficiency in essential tools like MS Office...Remote workFlexible hours
- ...Medical Monitor (US Board-Certified Oncologist) 3 days ago Be among the first 25... ...applicants Company Description PSI is a leading Contract Research Organization with 30 years in the... ...Monitors provide medical input to global clinical studies and advise the teams and...Full timeContract workWork from home
- ...Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform site management and ensure compliance... ...standards. Responsibilities include site qualification, monitoring, and documentation as well as acting as a liaison with study...Remote workFlexible hours
- Beth Israel Lahey Health in New Jersey is seeking a Clinical Research Coordinator responsible for screening and enrolling patients into clinical trials. The role involves monitoring protocol implementation and interacting with research subjects throughout their participation...Weekend workAfternoon shift
- ...Celerion is seeking a Full-time Nurse to assist with clinical research trials in Oklahoma. In this dynamic role, you will help with scheduled... ...include vital sign checks, ECGs, blood draws, and telemetry monitoring, along with reporting adverse events. The ideal candidate...Full time
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