Senior Clinical Research Associate Site Oversight & Monitoring
PAREXEL
Parexel is seeking a Clinical Research Associate in Raleigh, North Carolina, responsible for monitoring and ensuring proper conduct of clinical studies at allocated sites. The role requires close collaboration with local study teams, preparation for site initiation, compliance with ICH-GCP standards, and effective communication with investigators and site staff. A Bachelor’s degree in life sciences or related fields is necessary, along with strong negotiation and interpersonal skills. #J-18808-Ljbffr
- ...Grifols is seeking a Clinical Research Associate to manage clinical monitoring processes and ensure regulatory compliance. You will track study tasks, conduct monitoring visits, and facilitate investigator site interactions to support clinical trials. The ideal candidate...SeniorWebsite
- ...Syneos Health, Inc. is seeking an Experienced Clinical Research Associate based in Morrisville, NC. The role involves overseeing the integrity of clinical research studies, including site qualification and monitoring activities to ensure compliance with regulatory standards...SeniorWebsiteFlexible hours
- ...responsible for supporting monitoring and site management... ...with cross-functional clinical study teams and investigator... ...responsible for the oversight of activities... ...assess CRO Clinical Research Associate (CRA) and Investigator... ...experience for Senior CRA. Strong analytical...SeniorWebsiteInterim roleWork at officeLocal areaRemote work
$105.5k - $140k
...pulmonary hypertension associated with... ...You Are The Monitoring Team Lead/Senior Monitoring Team... ...implement and execute Clinical Monitoring activities... ...of study sites to ensure compliance... ...Assist Clinical Research Associates (CRAs... ...~4+ years of oversight and management of...SeniorWebsitePermanent employmentContract workWork at officeRemote work- ...A leading clinical research company in North Carolina is seeking a Clinical Research Associate to provide support for all clinical trials. The role involves preparing protocols, monitoring studies, and ensuring compliance with guidelines. Ideal candidates should have...Website
- Grifols, S.A is seeking a Clinical Research Associate in North Carolina to ensure site adherence to regulatory requirements and GCP Guidelines. You will manage site start-up and monitor clinical trials while maintaining project timelines and compliance. The ideal candidate...Website
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Raleigh, North Carolina. The Sr. CRA... ...Responsibilities include managing investigator site relationships, ensuring quality... ...and a minimum of 3 years of monitoring experience, preferably in Oncology....SeniorWebsite
- ...Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(... ...site and has the responsibility for monitoring the study conduct to ensure proper delivery...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
- Syneos Health is seeking an Experienced Clinical Research Associate in North Carolina to manage site-level activities, ensuring compliance with regulatory and... ...principles. You will perform site qualification, monitoring, and management activities, requiring exceptional...SeniorWebsite
- ...Job Summary The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(... ...site and has the responsibility for monitoring the study conduct to ensure proper...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
- Position: Senior Clinical Research Associate (level dependent on experience) Location: Raleigh, NC Job Id... ...What You’ll Do Manages investigative site activity for multiple protocols/... ...site visits (pre‑study, initiation, monitoring, and close‑out) and completes site visit...SeniorWebsiteLocal areaRemote workWork from homeHome office
- Syneos Health/ inVentiv Health Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site interactions and ensure safety and compliance within clinical trials. Responsibilities include managing project timelines, supporting team training, and maintaining...SeniorWebsite
- Ring Inc is seeking a Clinical Monitoring Operational Leader based in Raleigh, North Carolina, responsible for overseeing clinical trial execution. This role includes managing a dynamic team to ensure regulatory compliance and service quality across global studies. The...Website
$115k - $125k
...Senior Clinical Research Associate Piper Companies is currently seeking aSenior Clinical Research Associate (CRA) for an opportunity... ...Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities across multiple study Responsible...SeniorWebsiteRemote work- ...A leading Clinical Research Organization is seeking an experienced Senior Clinical Research Associate (CRA) for an opportunity in North Carolina. The role involves conducting site visits and monitoring activities across various studies. The ideal candidate will have 3-...SeniorWebsiteRemote work
$110.52k - $138.15k
...Sr. Clinical Research Associate - Central US ICON plc is a world-leading healthcare... ...clinical development. As a Senior CRA at ICON Plc, you will... ...will lead on clinical trial monitoring tasks requiring technical depth... ...Monitoring clinical trial sites to ensure adherence to...SeniorWebsiteFlexible hours- A clinical research organization in Raleigh, NC, seeks a Senior Clinical Research Associate to manage site activities for multiple protocols. The role requires a Bachelor’s or Master’s degree in health-related fields and offers substantial career support. You'll conduct...SeniorWebsiteRemote job
- ## Senior Clinical Research Associate - CNS/Rare Disease - Midwest - RemoteApplyremote type: Remotelocations: Research Triangle Park, North Carolinatime... ...management, and in-house CRAs for projects with heavy site management needs.Through regular touchpoints and coaching...SeniorWebsiteWork at officeRemote workWorldwide
- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate dedicated to overseeing clinical research site activities. This role involves performing site qualifications, managing compliance, and maintaining the integrity of clinical...SeniorWebsiteRemote job
- ...The Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols. Ensures coordination of an accelerated study start-up including...WebsiteInterim role
- ...Experienced Clinical Research Associate - Sponsor DedicatedSyneos Health is a leading fully integrated biopharmaceutical... ...like they belong.Job ResponsibilitiesPerforms site qualification, site initiation, interim monitoring, site management activities and close-out visits...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Clinical Research Associate II – Oncology (North Carolina/South Carolina) AbbVie’s mission is to discover... ..., partner with investigators and site staff, and drive performance. Job Description... ...site evaluation, training, routine monitoring, and closure activities in compliance...WebsiteContract workTemporary workLocal area
$105k - $118k
...Our Phase I team is currently seeking a Clinical Research Associate with 1+ year of experience. Ideal candidates should have Phase I experience... .... Responsibilities Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical...WebsiteWork at officeLocal areaNight shift$105k - $118k
...FTINC Fortrea Inc. is seeking a Clinical Research Associate who will be responsible for comprehensive site monitoring and management for Phase I clinical trials. The role requires at least 1 year of clinical monitoring experience and a relevant degree. Ideal candidates...Website- Clinical Research Associate (CRA) We are a global CRO dedicated to advancing clinical research. We are seeking a Clinical Research Associate to manage study sites across various therapeutic areas. Responsibilities Manage research activities at sites participating in clinical...SeniorWebsiteRemote jobWork at officeWorldwide
- Clinical Research Associate Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, ensuring compliance with regulatory... ...properly and report safety‑related events. Monitor site activities during study maintenance and...SeniorWebsiteRemote jobContract workWork at officeWorldwide
- ...long and successful career!ELS is hiring for the position of Pool Monitor in Stella, North Carolina.**What you’ll do:**The Pool Monitor... ...environment.* Strong attention to detail.We invite you to visit our web site at for additional information regarding our exceptional resort...WebsiteLocal area
- Objective As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial... ...study feasibility assessments, and site selection processes Assist in the preparation... ...) and study manuals Clinical Trial Monitoring: Conduct site qualification, site...WebsiteInterim roleLive inLocal areaRemote work
- Clinical Research Associate Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practice (GPP...WebsiteInterim roleLocal areaRemote workFlexible hours
- ...Country Lead Monitor ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation... ..., among others. Visit our careers site to read more about the benefits ICON offers....WebsiteLocal areaFlexible hours
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