CRA I - Oncology Clinical Monitor (On-site)
IQVIA
IQVIA Biotech is hiring a Clinical Research Associate I (CRA I) to support on-site monitoring in oncology trials. The CRA I ensures protocol compliance, data integrity, and patient safety across clinical study sites, with travel as required. The role emphasizes monitoring visits, TMF/ISF maintenance, and collaboration with internal teams to drive study execution and enrollment targets. Bachelor’s degree and GCP/ICH knowledge are preferred, with 6 months to 2 years of CRA experience and travel #J-18808-Ljbffr IQVIA
- Emmes Group in Rockville, MD seeks a Senior In-House CRA to support site management and monitoring of clinical studies, ensuring trials are conducted and reported per protocol and SOPs. The role may involve program-level status tracking across multiple studies. Ideal candidates...Website
- IQVIA is seeking a Clinical Research Associate (CRA) in Rockville, MD to enhance clinical trial quality. The CRA will lead site monitoring visits, ensuring compliance and building relationships with sites for effective study delivery. Ideal candidates hold a Bachelor’s...Website
- The Emmes Company, LLC is looking for a Clinical Research Associate II to monitor clinical study sites both onsite and remotely. The successful candidate will ensure compliance with protocols, conduct monitoring activities, document observations, and provide training to...WebsiteRemote jobWork from homeFlexible hours
- Emmes Group is seeking a Clinical Research Associate II in Rockville, Maryland. The successful... ...and conducting remote and onsite monitoring visits, ensuring compliance with protocols... ...observations. You will also assist in training site staff and develop patient recruitment...WebsiteRemote job
- 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...WebsiteRemote job
- Emmes is seeking a Clinical Research Associate II to monitor clinical study sites either remotely or onsite. The role involves ensuring compliance with clinical protocols, documenting monitoring activities, and training site staff. Candidates should have a Bachelor’s degree...WebsiteRemote jobFlexible hours
- Emmes is seeking a Senior Clinical Research Associate to monitor clinical study sites in Rockville, Maryland. This role involves ensuring compliance with protocols, conducting remote and on-site visits, and training site staff on GCP. The ideal candidate will have a Bachelor...WebsiteRemote job
- Emmes Group seeks a Senior Clinical Research Associate to monitor clinical sites remotely or on-site, ensuring trials are conducted per protocol and ICH GCP. You will support site selection, site visits, data verification, and regulatory documentation across diverse therapeutic...WebsiteRemote job
$130k - $216k
...Job Family : Clinical Trial Operations Travel Required : None Clearance Required... ...searching for a Clinical Trials Program Monitor and Auditor to independently provide support... ...(NIAID). This is a full-time, on-site opportunity in Bethesda, MD. Schedule...WebsiteFull timeTemporary workInterim roleFlexible hours- The Emmes Group is seeking a Sr. In-House CRA to support site management and monitoring of clinical studies, ensuring trials are conducted per protocol and regulatory requirements. The role involves documentation, IRB submissions, and cross-functional collaboration. The...WebsiteRemote job
- Emmes Group, a leading CRO, is seeking a Sr. In-House CRA to support site management and monitoring of clinical studies from Rockville, MD. You will ensure trials are conducted, recorded, and reported per protocol and regulatory requirements. You will maintain trial master...WebsiteRemote job
$93.1k - $232.8k
...patients faster.Drive global clinical trials from first site activation to final... ...experience (Phase III required)Oncology experience required... ...site selection, activation, monitoring oversight, and closeout—while... ...functional project teamsSupport CRA and team training on...WebsiteFull timeContract workPart timeWork at officeImmediate startWorldwide$157k - $186k
...Associate Director, Drug Safety and Medical Monitoring is responsible for leading medical... ...and medical review activities across all clinical trials, as well as overseeing patient safety... ...inquiries and questions from the sites/CRA/study team. Develop, implement, and update...WebsiteFull timeContract workWorldwideVisa sponsorship$50k - $70k
Piper Companies is seeking a Clinical Research Associate (CRA) to support the operational delivery of clinical trials in Bethesda, MD. This hybrid role serves as a key liaison between investigative sites and study teams, driving performance, regulatory compliance, and...Website- Overview Ophthalmology Strategy and Medical Monitor US Remote Emmes Group: Building a... ...Emmes Group is transforming the future of clinical research, bringing the promise of new medical... ...Key Opinion Leaders (KOLs), site investigators, reading centers, imaging vendors...WebsiteContract workWork experience placementCasual workLocal areaRemote workWork from homeFlexible hours
$131k - $155k
...Senior Manager of Drug Safety and Medical Monitor will provide medical monitoring support... ...team. They will conduct medical reviews of clinical research data, safety alerts and... ...Safety Management Plans, and participate in Site Initiation Visits. Provide medical input...WebsiteFull timeVisa sponsorship$284.38k - $426.57k
Executive Director, Clinical Development Operations (Early Oncology)The Executive Director, Clinical Operations, is... ...implement AI/digital solutions and monitor industry innovations to ensure the... ...to monitor performance, optimize site selection, and accelerate study start...WebsiteHourly payFull timeTemporary work- Emmes Group in Rockville, Maryland, is seeking a Medical Officer to oversee medical monitoring of clinical trials and ensure safety efficacy compliance. Responsibilities include evaluating adverse events and providing medical input during protocol development. The ideal...Remote jobFlexible hours
$50k - $70k
Piper Companies is seeking a Clinical Research Associate (CRA) to support the... ...across infectious disease, oncology, and cardiology programs.... ...liaison between investigative sites and study teams, driving site... ...activities, including remote monitoring, site communication, and...WebsiteRemote work$120k - $140k
...Job Details Remote Senior CRA position in the oncology space. Jobot Job is hosted... ...Develops strong investigative site relationships and ensures... ...initiation visits, interim monitoring visits, and close‑out visits... .... Works with in‑house Clinical Trial Assistant to collect,...WebsiteInterim roleLocal areaRemote workFlexible hours- ...behavior analytics, or patient privacy monitoring platforms.• Certifications such as CISSP... .... Hybrid: minimum of 2 days per week on-site.QualificationsMinimum EducationBachelor'... ...changeIdentify opportunities to improve clinical and administrative processesMake appropriate...WebsiteWork experience placement2 days per week
$58.8k - $77.44k
Overview Join Our Team at Maryland Oncology Hematology! We're looking for... ..., and enrolling patient in clinical trials. CRC II also... ...financial information. Assures site research quality by practicing... .... May assist with scheduling monitoring and auditing visits, and interact...WebsiteWork experience placementWork at officeLocal area- Precigen is seeking a highly motivated and skilled Head of Clinical Operations(level determined by candidate experience), to drive our... ...develop next generation gene and cell therapies focused in immuno-oncology, autoimmune disorders, and infectious diseases. Reporting to...Website
- IQVIA is seeking a Global Study Manager to drive end-to-end site management for global oncology trials. You will lead site identification, activation, monitoring, and closeout while balancing speed, quality, and cost. You will partner with cross-functional teams, manage...Website
- Guidehouse in Bethesda, MD is seeking a Clinical Research Coordinator to manage oncology and cancer-related trials on-site. The role involves coordinating multiple studies, onboarding staff, and ensuring data integrity in EMR/CTMS/EDC systems, while adhering to FDA/ICH...Website
$151.23k - $226.84k
...digital health strategy can be found here. Oncology is the largest therapeutic area within... ...Excellence, will have experience in the use of clinical outcomes assessments (COA) such as... ...professionals and care teams at clinical trial sites do not want a fragmented approach. They...WebsiteHourly payFull timeTemporary workWork at office3 days per week- ...Laboratory for Cancer Research, Bethesda, MD, seeks a clinical research nurse to support NIH oncology trials. This exempt full-time role provides clinical supervision... ...compliance with ICH/GCP and regulatory standards. On-site at NIH Clinical Center is required; telework may be...WebsiteFull timeRemote work
- Dovel Technologies, Inc. is seeking a Clinical Research Coordinator to support oncology trials at the National Cancer Institute in Bethesda, MD. This full-time, on-site position requires coordinating multiple studies, training junior staff, and ensuring regulatory readiness...WebsiteFull time
$90.2k - $175.1k
Join a Team That’s Advancing Clinical ResearchWe’re looking for a passionate... ...Clinical Research Associate (CRA) to join our team and play a... ...ll partner with investigative sites and cross-functional teams to... ...’ll DoLead and execute site monitoring visits (selection, initiation,...WebsiteFull timePart timeImmediate startWorldwide- A biotech company in Germantown, MD is seeking a Remote Senior CRA to advance oncology trials. This role involves building strong site relationships, conducting compliance visits, and outstanding monitoring responsibilities. Candidates should have prior oncology experience...WebsiteRemote jobFlexible hours
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