In-House Clinical Research Associate — TMF Mastery & FDA/GCP
Experis
Experis is seeking an In-House Clinical Research Associate to join our client’s Clinical Operations team in Bethesda, Maryland. The role supports research and development efforts, requiring strong organizational and communication skills and a proactive approach. You will review regulatory documents, maintain TMF, track documents in a centralized system, ensure FDA/ICH GCP compliance, and contribute to high-quality clinical trials within a collaborative environment that values diversity and #J-18808-Ljbffr Experis
$50k - $80k
Piper Companies is seeking an In-House Clinical Research Associate located in Bethesda, MD. The role involves reviewing and processing regulatory... ...Trial Master Files, and ensuring compliance with FDA and ICH GCP guidelines. Ideal candidates will have 3-5 years of experience...House- ...Clinical Research AssociateOur client, a leading organization in the... ...is seeking a dedicated In-House Clinical Research Associate to join their team. As a... ...organize Trial Master Files (TMF) and centralized document... ...documents meet FDA, ICH GCP, and sponsor requirements...HouseFlexible hours
- ...Job Title In-House Clinical Research Associate Location Bethesda, MD 20817 US (Primary) Category... ...sites for the Trial Master File (TMF) or another central documents file... ...and completeness as required by FDA regulations, ICH GCP, Sponsor requirements, and...HouseFull timeWork at officeLocal areaRemote work
$50k - $80k
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...HouseWork at office$50k - $80k
Piper Companies is looking for an In-House Clinical Research Associate to join a clinical research company... ...Maintain and organize Trial Master Files (TMF) and centralized document systems... ...or database Ensure documents meet FDA, ICH GCP, and sponsor requirements for...HouseWork at office- ManpowerGroup is seeking an In-House Clinical Research Associate to join the Clinical Operations team in Bethesda... ...role supports regulatory processes, TMF maintenance, and R&D efforts, with... ...research experience, knowledge of FDA and ICH GCP guidelines, and hands-on experience...House
$50k - $70k
Piper Companies is seeking a Clinical Research Associate (CRA) to support the... ...maintain compliance with ICH-GCP and SOPs. Qualifications of... ...(CRO, sponsor, or site), in-house preferred. Prior experience... ...Strong knowledge of ICH-GCP, FDA regulations, and clinical trial...HouseRemote work- ...Overview Clinical Research Associate I Be Part of One Team, One Purpose. At Emmes Group, we’re... ...standard operating procedures (SOPs), ICH GCP, and all applicable regulatory... ...clinical research experience (as a CTA, in-house CRA, CRC etc.) preferred Preferred ~...HouseWork experience placementInterim roleCasual workLocal areaRemote workWork from homeFlexible hours
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Washington DCICON is a global healthcare intelligence and... ...essential document collection and TMF reconciliation with site filesSupport... ...working within a Functional Services (or in-house) monitoring model is preferredWilling...HouseInterim roleLocal areaRemote work- ...the world's health. From clinical trials to regulatory,... ...seeking a Senior Clinical Research Associate or Clinical Research... ...Good Clinical Practices (GCP), and sponsor standards... ...to Trial Master File (TMF) documentation, site... ...and Drug Administration (FDA) and local country regulationsMust...Full timeLocal areaRemote work
- ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a... ...remotely) ensuring regulatory, ICH-GCP and/or Good... ...with the Trial Master File (TMF). Ensures the investigator/physician... ...worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...full-service Contract Research Organization (CRO) supporting... ...With expertise across Clinical Operations, Biometrics,... ...Clinical Research Associates (CRAs) to support future... ...in accordance with ICH-GCP and regulatory requirementsSite... ...and Trial Master File (TMF) managementSite...Contract workWorldwide
- Description Clinical Research Associate Venesco LLC is seeking a Clinical Research Associate (CRA) to provide clinical monitoring and oversight... ...conducted in compliance with protocols, Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and sponsor requirements....
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions... ...or remotely) ensuring regulatory, ICH ‑GCP and/or Good Pharmacoepidemiology Practice... ...it with the Trial Master File (TMF), and ensure sites are aware of archiving...Interim roleLocal areaImmediate startRemote workFlexible hours
- Guidehouse is seeking a Clinical Study Laboratory Coordinator to support NIH projects in Bethesda, MD. The role interfaces with principal... ..., protocol navigators, and laboratory staff to manage in-house and reference testing for clinical studies. The ideal candidate...House
- ...Research Project AssociateInova Juniper Program is looking for... ...dedicated Research Project Associate to join the team. This full... ...budgetary records. Adheres to ICH- GCP, DHHS (OHRP and FDA) as well as Inova Health... ..., administrative or clinical support rolePreferred Qualifications...Full timeMonday to FridayFlexible hoursShift workDay shift
$90k - $120k
...Clinical Research AssociateRockville, MarylandMedical Organization – Clinical Operations... ...a Clinical Research Associate (CRA), you will be responsible for... ...review & cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs. You'll act as...Full timeWork experience placementSummer work$83k - $114.2k
...As the Clinical Research Associate II, you will be responsible for planning, execution and oversight of... ...clinical studies in compliance with ICH-GCP and IVD clinical guidelines, applicable... ...clinical research. Deep knowledge of FDA clinical research regulations, and ICH-...Full timeTemporary workWork experience placementWork at office- ...seeking an Animal Health Technician II to provide surgical and clinical support under supervision. The role requires experience in laboratory... ...school diploma or equivalent and knowledge of animal species housed in the facility. This full-time position may require weekend...HouseFull timeShift workWeekend work
- ...Will DoExpert in the field of drug research and development, contributing... ...expertise to guide the full lifecycle of clinical research and development projects... .... • Manage activities associated with audits to ensure compliance with GCP, ICH, AZ standards, and local/international...Full timeLocal area
- Emmes Group in Rockville, MD is seeking a Clinical Research Associate I to monitor clinical study sites, conduct site visits, and ensure trials comply with protocol, SOPs, ICH GCP, and regulatory requirements. You will perform site visits, informed consent reviews, source...Remote job
$48k - $58k
Piper Clinical Solutions is seeking a Clinical Research Assistant in the Bethesda, MD area to support a well-established... ...clinical research studies associated with protocols and abstractions Requirements... ...include: Experience with IRB/GCP regulations Bachelor’s Degree in...- Piper Clinical Solutions in Bethesda, MD is seeking a Clinical Research Assistant to support a CRO focused on biopharmaceutical development, health information services... ...protocol data for trials. Requires IRB/GCP experience and a science degree (Master’s preferred...
- Clinical Research Associate II Emmes Group is a full-service contract research organization (CRO) that modernises clinical trials and accelerates... ...conduct the study in compliance with the protocol, SOPs, ICH GCP and applicable regulations. Provide training and re-...Contract workInterim roleRemote work
- Senior Clinical Research Associate At Emmes Group, we’re shaping the future of clinical research—where human intelligence meets cutting‑edge technology... ..., and reported in accordance with the protocol, SOPs, ICH GCP, and all applicable regulatory requirements....Work experience placementInterim roleRemote work
- ...provide surgical, technical, and clinical support services under the... ...be related to the species housed in the Building 49 CAF. Animal... ...be certified by the American Association for Laboratory Animal Science... ...dictated by the institutional research schedule, weekend and holiday...HousePermanent employmentContract workWork experience placement
- ManpowerGroup Global, Inc. is seeking an In-House Clinical Research Associate in Bethesda, MD to support clinical operations. The role emphasizes regulatory document review, TMF management, and ensuring FDA/ICH GCP compliance. You will coordinate documentation, maintain...House
- Emmes Group is seeking a Clinical Research Associate II to monitor clinical trial sites, either onsite or remotely, ensuring trials are conducted, recorded, and reported per the protocol and ICH GCP. You will conduct visits, perform ICF reviews, SDV, AE tracking, and site...Remote job
- Emmes is seeking a Senior Clinical Research Associate to monitor clinical study sites in Rockville, Maryland. This role involves ensuring compliance... ...remote and on-site visits, and training site staff on GCP. The ideal candidate will have a Bachelor’s Degree in a scientific...Remote job
$27 per hour
...monitoring, and husbandry of research animals, with a focus on rodents... ..., and troubleshoot aquatic housing equipment. Maintain accurate... ...services to support our clients' clinical laboratory testing needs and... ...Food and Drug Administration (FDA) in the past five years. We...HouseHourly payContract workLocal areaWorldwideFlexible hours
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