Senior Clinical Research Associate Site & Study Oversight
Worldwide Clinical Trials Holdings, Inc.
Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate to manage research activities for clinical projects across various sites. The role involves overseeing site activities, ensuring compliance with regulations, and training teams to collect data accurately. The ideal candidate should possess a 4-year degree or RN/BSN in Nursing, have over 5 years of relevant experience, and excellent organizational skills. This position requires some travel to various locations. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.
- ...supporting monitoring and site management... ...client Sponsored studies. Site monitoring... ...cross-functional clinical study teams and... ...responsible for the oversight of activities... ...assess CRO Clinical Research Associate (CRA) and... ...related experience for Senior CRA. Strong analytical...SeniorWebsiteInterim roleWork at officeLocal areaRemote work
- ## Senior Clinical Research Associate - Psychiatry - East Coast - RemoteApplyremote type: Remotelocations: Research... ...-house CRAs for projects with heavy site management needs.Through regular... ...involved in all stages of the clinical study, including identifying potential...SeniorWebsiteWork at officeRemote workWorldwide
$120k - $140k
...We are looking for 1-2 Senior CRA's to join our team!... ...Develops strong investigative site relationships and... ...but not limited to Pre-study visits, initiation... ...and on-site monitoring & oversight activities using various... ...management Work with in-house Clinical Trial Assistant to...SeniorWebsiteInterim roleLocal areaRemote workFlexible hours- ...Experience required. Cell therapy experience is strongly preferred. 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(s). The CRA works in close...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
- 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
- Responsibilities Managing research activities at sites participating in Worldwide’s clinical research projects, predominantly registries... ...-interventional/observational studies. Involving in all stages of... ...as a Clinical Research Associate. A 4-year university degree or...SeniorWebsiteRemote jobWork at officeWorldwide
- ABOUT THE JOB The Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring... ...WHAT YOU WILL DO: Monitor clinical studies of investigational and approved... ..., initiation, interim, and close‑out site visits. Manage and train site personnel...SeniorWebsiteInterim roleWork at office
- Position: Senior Clinical Research Associate (level dependent on experience) Location: Raleigh, NC Job Id:... ...department can provide an update on a study or milestone that they have achieved.... ...What You’ll Do Manages investigative site activity for multiple protocols/...SeniorWebsiteLocal areaRemote workWork from homeHome office
- 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
$115k - $125k
Senior Clinical Research Associate Piper Companies is currently seeking aSenior Clinical Research Associate (CRA) for an opportunity in North Carolina... ...Research Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities across...SeniorWebsiteRemote work- Syneos Health/ inVentiv Health Commercial LLC is hiring an Experienced Clinical Research Associate in North Carolina. This role involves site management, regulatory compliance, and ensuring that clinical trials operate smoothly. Candidates should have a Bachelor's degree...SeniorWebsiteRemote jobFlexible hours
- Sr. Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical... ...of clinical development. As a Senior CRA at ICON Plc, you will oversee... .... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements...SeniorWebsiteFlexible hours
- The Clinical Research Associate (CRA) is responsible for the site management, site monitoring and close-out of assigned clinical... ...patient safety and quality study execution in accordance with applicable... ...timelines Ensure adequate oversight of the investigational product at...WebsiteLocal areaRemote work
- ...America) Please review the following job description: The Senior Capital Oversight Risk Manager serves as a senior subject matter expert,... ...Truist's generous benefit plans, please visit our Benefits site ( . Depending on the position and division, this job may also...SeniorWebsiteFull timePart timeShift workDay shift
$70.1k - $126.1k
...home-based role in Morrisville, NC. The responsibilities include site qualification, monitoring, and management activities, ensuring... ...possess strong communication skills, and have knowledge of Good Clinical Practice guidelines. The position offers a competitive salary range...SeniorWebsiteRemote jobWork from homeFlexible hours- A leading biopharmaceutical solutions organization is seeking an Experienced Clinical Research Associate to oversee site monitoring, ensuring compliance with regulatory requirements and clinical protocols. Responsibilities include conducting site visits, managing site activities...SeniorWebsiteRemote jobWorldwide
- ...a high school diploma or GED and at least one year of experience in a construction inspector role. A valid North Carolina driver's license is also required. This position involves travel between different CFPUA sites. #J-18808-Ljbffr Cape Fear Public Utility AuthoritySeniorWebsite
- ...on 07/27/2024 Responsible for providing Clinical Research support for all clinical trials. Under the... ...will serve as support for the clinical study team. Participate and assist in design... ...in the evaluation of potential clinical sites according to established criteria of acceptability...Website
- 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
- 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... ...improving data integrity, compliance, study performance, and the customer...WebsiteContract workTemporary workLocal area
$55k - $65k
...We are currently hiring an In‑House Clinical Research Associate to join our team! As an In‑House CRA here... ...and data reviews to ensure that studies operate in compliance with study protocols... ...Collect, track and review investigational site records relating to subject screening...WebsiteHourly payWork experience placementCurrently hiringLocal areaRemote work- Overview Experienced Clinical Research Associate - Full-Service Syneos Health is a leading fully integrated... ...belong. Responsibilities Performs site qualification, site initiation, interim... ...the effective conduct of the clinical study data review and capture. Verifies site...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- 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 a...Website
- ...ECS) is seeking an experienced Senior Project Manager to join our... ...Scheduling, training and oversight of subordinate staff members... ...routine visits to active project sites to ensure appropriate quality... ...findings and conclusions in studies. Communicate with junior staff...SeniorWebsiteFor subcontractorLocal area
- ...is seeking to a hire a Senior Electrical Engineer. We... ...design. From groundbreaking research labs to innovative... ...and provide technical oversight. Review and approve... ...RFIs. Conduct targeted site visits to resolve... ...neighbors work, create, study, perform, and dream....SeniorWebsiteWork at office
- ...Patient Safety team as a Senior Physician where you'... ...of patients in clinical trials and post-marketing... ...to Parexel staff or site (investigator/study coordinator), as... ...documents Providing oversight and relevant inputs to... ...epidemiology background research Provide safety...SeniorWebsiteInternshipWork at officeLocal areaRemote workWork from homeFlexible hours
$122k
Overview Premier Research is looking for a Senior Trial Manager (Sponsor... ...overseeing and managing clinical trials for biotech,... ...Provide oversight and trial management... ...Documents, templates, and study plans. Contribute to... ...CRAs and investigative sites. Create and maintain...SeniorWebsite- Wake Research seeks a Clinical Research Coordinator II in Raleigh, NC. This role involves managing day-to-day activities of clinical trials,... ...also includes mentoring research staff and contributing to study oversight. Benefits include competitive wages, health insurance,...Senior
- ...for implementation of one or more clinical trials and all activities from study start-up through database lock, ensuring... ..., and operational aspects of site investigator grants and grant... ...clinical trials as needed Provides oversight to staff maintaining clinical trial...SeniorWebsiteContract workRemote work
$310k - $375k
...Senior Medical Director - Clinical Research About Pharming Pharming Healthcare Inc. is a global biopharmaceutical... ...(strategy, develop protocols, study start-up, close-out, oversight, and regulatory support) for... ...Lead clinical study site engagement in the US...SeniorWebsiteTemporary workWork experience placementRemote workFlexible hours
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