In-House Clinical Research Associate — TMF & Regulatory
$50k - $80kTechnical Resources International Inc
Technical Resources International, Inc. in Bethesda, MD is seeking an In-House Clinical Research Associate to support clinical study teams with regulatory document management and compliance tasks. The ideal candidate holds a Bachelor's Degree and possesses excellent negotiation, communication, and organizational skills. The role demands proficiency in Microsoft Office and may involve regulatory document review experience. The salary range is $50,000-$80,000 annually, with no travel required. #J-18808-Ljbffr Technical Resources International, Inc.
$50k - $80k
Piper Companies is seeking an In-House Clinical Research Associate located in Bethesda, MD. The role involves reviewing and processing regulatory documents, maintaining Trial Master Files, and ensuring compliance with FDA and ICH GCP guidelines. Ideal candidates will have...HouseRegulatory- ...Job Title In-House Clinical Research Associate Location Bethesda, MD 20817 US (Primary) Category... ...Retrieve, file, and maintain essential regulatory documents from clinical trial sites for the Trial Master File (TMF) or another central documents file platform...HouseRegulatoryFull timeWork at officeLocal areaRemote work
$50k - $80k
Piper Companies is looking for an In-House Clinical Research Associate to join a clinical research company... ...Responsibilities Review and process essential regulatory documents received from clinical... ...and organize Trial Master Files (TMF) and centralized document systems...HouseRegulatoryWork at office$50k - $70k
Piper Companies is seeking a Clinical Research Associate (CRA) to support the operational delivery of... ...study teams, driving site performance, regulatory compliance, and data quality. This... ...experience (CRO, sponsor, or site), in-house preferred. Prior experience in in-house...HouseRegulatoryRemote work$120k - $140k
...Sr. Oncology Clinical Research Associate opportunity! This Jobot Job is hosted by: Audrey Block Are you... ..., reviews, and monitors required regulatory documents for study start-up, study maintenance... ...to upper management Work with in-house Clinical Trial Assistant to collect,...HouseRegulatoryInterim roleLocal areaRemote workFlexible hours$70k - $115k
...Clinical Research Associate The Clinical Research Associate (CRA) is primarily responsible for ensuring... ...ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client... ...or PM. In collaboration with the In-house Clinical Research Associate (IHCRA) and...HouseRegulatoryContract workLocal areaRemote workWorldwideFlexible hours- Dexian DISYS in Rockville, MD is seeking an In-House Clinical Research Associate (CRA) to manage essential regulatory documents for clinical trials. The role requires candidates to work 2 days on-site while offering a hybrid work environment. You will ensure the accuracy...HouseRegulatory
- Experienced Clinical Research Associate - Full-Service Syneos Health is a leading fully integrated biopharmaceutical... ...on-site or remotely) ensuring regulatory, ICH-GCP and/or Good... ...the ISF with the Trial Master File (TMF). Ensures the investigator/physician...RegulatoryContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Job Purpose The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site... ...not limited to Trial Master File (TMF) documentation, site reports, site follow... ...knowledge of global and local regulatory requirements. Demonstrated understanding...RegulatoryLocal areaRemote work
$20 - $27 per hour
...Piper Solutions is seeking a TMF Specialist to support our client... ...(TMF) across one or more clinical studies, ensuring compliance... ...specifications, ICH/GCP, and regulatory requirements Perform QC review... ...Operations, Clinical Trials, Clinical Research, ICH‑GCP, GCP Compliance, FDA...Regulatory- ...NIH Branch. The attorney will provide in‑house counsel on intellectual property matters... ...legal advice on compliance oversight, regulatory drafting, litigation, and organ procurement... ...OGC attorneys and report to the Deputy Associate General Counsel for Public Health....HouseRegulatoryWork at office
- ...Position: Senior Clinical Research Associate (level dependent on experience) Location: Washington, DC Job Id: CRA ongoing WA # of Openings... ...form (CRF) retrieval / source document review (SCV), regulatory documents, and investigational product. Participates...RegulatoryLocal areaRemote workWork from homeHome office
$40k - $50k
A clinical research organization is seeking a TMF Specialist in Bethesda, MD, for a hybrid role with three remote days weekly. The successful candidate will manage TMF set-up, document quality, and regulatory compliance. Applicants should have at least one year of TMF...RegulatoryRemote job$50k - $70k
Piper Companies is seeking a Clinical Trial Specialist (IRB) for a short-term assignment in Bethesda... ...clinical trial operations by ensuring the TMF is compliant and audit-ready. The ideal candidate will have 1-3+ years of regulatory IRB experience and strong database skills....RegulatoryTemporary work$73.6k - $85k
...Clinical Research Associate Responsible for assessing the study capabilities of potential study sites, training, on-site monitoring, closure... ...Forms, and resolving all data queries Review the regulatory binder and essential documents at the site and verify all...RegulatoryFull timeWork experience placementInterim roleWork at officeLocal areaRemote workNight shift- ...therapy experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the... ...as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits,...RegulatoryLocal areaRemote workFlexible hoursShift work
$47.59k - $87.56k
...Overview The candidate will provide clinical and research services to clinical trial subjects... ...clinical situations. The Clinical Research Associate works directly with clinical trial... ...to ensure objectives are met and regulatory compliance is maintained Collaborates...RegulatoryHourly payWork experience placementWork at office- Overview Clinical Research Associate II US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming... ...operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. The CRA will conduct monitoring visits and...RegulatoryWork experience placementInterim roleCasual workLocal areaRemote workWork from homeFlexible hours
- ...support the financial operations of a portfolio of affordable housing communities. This role is ideal for a detail-oriented accounting... ...HUD REAC submissions and ensure compliance with state and regulatory reporting requirements Coordinate with lenders and investors...HouseRegulatoryFull time
$87.56k
Georgetown University in Qatar seeks a Clinical Research Associate to provide clinical and research services for Infectious Diseases studies in... ...-19 studies and monitoring trial subjects while ensuring regulatory compliance. The ideal candidate will have a Bachelor’s...Regulatory- ...Clinical Research Coordinator Live and work in a thriving urban center near the nation's capital... ...a local church, the Bethesda Meeting House (1820, rebuilt 1849), which in turn... ...protocols, is ethically-conducted and follows regulatory standards Maintaining research...HouseRegulatoryLocal area
- ...divh2Clinical Research Associate - California/h2pICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and... ...they are conducted according to protocol, regulatory requirements, and industry standards./ppWhat...Regulatory
$40k - $50k
Overview Piper Companies is looking for a TMF Specialist to join a clinical research organization (CRO). This is a hybrid position with 3 remote days out... ...with eTMF specifications, ICH/GCP guidelines, regulatory requirements, and applicable SOPs. Ensures that all new...RegulatoryRemote work3 days per week- ...involves collaboration with cross-functional clinical study teams and investigator site... ..., monitoring plan, ICH GCP, local regulatory requirements, and client SOPs. Conduct... ...of study metrics, assess CRO Clinical Research Associate (CRA) and Investigator Site performance...RegulatoryInterim roleWork at officeLocal areaRemote work
$22.16 - $32.93 per hour
Join the HJF Team! HJF is seeking a Clinical Research Assistant II - DARPA to support clinical research evaluating novel interventions to... ...recruitment, screening, data collection, protocol adherence, and regulatory compliance for a clinical trial that combines brain...RegulatoryHourly payFor contractorsHome office- ...eligible for a $75,000 recruitment incentive in accordance with regulatory requirements. Click apply to view full details and eligibility... ...protection. Duties include: Providing protection for The White House Complex, The Vice President's Residence, The Main Treasury...HouseRegulatory
$150k - $180k
...Associate Counsel Bethesda, MD Work on products that matter. ProShares, a leading sponsor... ...ongoing disclosure, reporting, and regulatory engagementwith high visibility, real accountability... ...: ~3 or more years of law firm or in-house legal experience with a focus on mutual...HouseRegulatory$60k - $80k
...Chase Trust Client Services Associate Chevy Chase Trust is a privately... ...unique thematic investment research and asset management. Chevy... ...usage of modern in-house fitness center ~ On-premise... ...firm policies, procedures and regulatory guidelines Utilize internal...HouseRegulatoryWork experience placementWork at office$90k - $120k
...specializes in unique thematic investment research and asset management. Chevy Chase Trust... ...~ Complimentary usage of modern in-house fitness center ~ On-premise full-service... ...internal and external audit reviews and other regulatory reporting as needed. Reconciliation:...HouseRegulatoryTemporary workWork at office$90k - $130k
...and assure compliance with OSHA and other regulatory requirements (e.g., signs, permits,... ...Training Attend as assigned all CWC in-house and external training programs. Participate... ...job demands, or working conditions associated with the job. Successful candidates will...HouseRegulatoryFull timeFor contractorsFor subcontractorWork at officeLocal areaImmediate startNight shiftWeekend work
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