In-House CRA: Trial Monitoring & Documentation
The Emmes Company, LLC
The Emmes Company, LLC is hiring an In-House Clinical Research Associate to assist with operational activities for clinical trials. This role involves site management, monitoring, and ensuring compliance with protocols and regulatory requirements. The ideal candidate has a Bachelor’s Degree in a scientific discipline and may have less than a year of clinical research experience. Proficiency in MS Office and strong organizational skills are essential for success. #J-18808-Ljbffr The Emmes Company, LLC
- Emmes Group is seeking an In-House Clinical Research Associate to support operational activities for clinical trials. The role involves assisting project teams in tracking trial progress and ensuring compliance with protocols and regulatory standards. The ideal candidate...House
- ...better future for us all. Overview In-House CRA II US Remote Emmes Group: Building... ...the site management and monitoring of clinical studies/trials, ensuring clinical trials are conducted... ...enrollment updates, questions, missing documentation, meeting arrangements, etc....HouseRemote jobWork experience placementInterim roleCasual workLocal areaWork from homeFlexible hours
- ...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’...Suggested
- Hybrid In-House CRA Posted: 18 May 2026 Location: Rockville, MD Reference: 100... ..., and maintain essential regulatory documents from clinical trial sites for the Trial Master File (TMF... ...materials to study sites. May assist in monitoring visit preparation and/or follow up...HouseWork at office
- 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...SuggestedRemote jobFlexible hours
- Overview Clinical Trial Manager II US Remote... ...CTM II will lead the monitoring team and associated deliverables... ...oversight for in-house Clinical Research... ...other participant-facing documents, site training materials... ...deliverables are met by CRA staff, including, but not...HouseCasual workLocal areaRemote workWork from homeFlexible hours
$18.5 per hour
...Rochambeau), has an immediate opening for a BUS MONITOR - Part-Time for the 2026-2027 school... ...grade. Our school thrives on diversity, housing over 80 nationalities. We steadfastly... ...accurate and timely records and documentation, including notes on disciplinary issues...HouseHourly payPart timeImmediate startShift work- Overview Ophthalmology Strategy and Medical Monitor US Remote Emmes Group: Building... ...for medical monitoring of ophthalmology trials; scientific and clinical oversight of... .... Clinical and Scientific Document Development Provides medical input...Contract workWork experience placementCasual workLocal areaRemote workWork from homeFlexible hours
$85k - $125k
...Companies is looking for a Central Monitor to join a clinical research... ..., and tools for corporate and trial-specific use Review study... ...and provide recommendations for CRA follow-up Train project teams... ...strategies Ensure adherence to documented processes and timelines, and take...Remote workShift work$85k - $115k
Job Title Central Monitor Location Bethesda, MD 20817 US (Primary... ...and for applicable clinical trials. Review protocols to ensure... ...potential issues/mitigation. Ensure documentation of processes and workflows... ...Prior experience as a CRA conducting on-site monitoring...Full timeContract workLocal areaRemote workRelocationShift work$85k - $125k
A clinical research organization in Bethesda, MD is seeking a Central Monitor to oversee risk-based quality management in clinical trials. Candidates should have a strong background in regulatory requirements and a minimum of 3 years in centralized monitoring. Responsibilities...$120k - $140k
...Associate focused on oncology with responsibilities including site monitoring, regulatory oversight, and ensuring compliance with protocols.... ...the time. The ideal candidate will have experience in clinical trials and regulatory frameworks, strong communication skills, and the...Remote job- ...seeking an Ophthalmology Strategy and Medical Monitor. This role involves strategic medical leadership and oversight of ophthalmology trials, focusing on safety and efficacy. The... ...include ensuring high-quality clinical documents, interfacing with experts, and supporting...Remote workFlexible 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...House
- ...research organization is seeking an Ophthalmology Strategy and Medical Monitor to provide strategic leadership for clinical development programs. This role focuses on medical monitoring of ophthalmology trials, ensuring safety and efficacy through collaboration with experts...Remote work
- Overview In-House Clinical Research Associate... ...modernizing clinical trials and accelerating the development... ...Research Associate (CRA) is responsible for... ...site management and monitoring of clinical studies/... ...updates, questions, missing documentation, meeting arrangements,...HouseInterim roleLocal areaRemote work
- ...Technical Resources International, Inc. is seeking a Central Monitor to oversee risk-based quality management and centralized monitoring processes. This role requires a Bachelor's degree and a minimum of 3 years of relevant experience in a CRO setting. Candidates should...Remote workRelocation
- Regulatory Monitoring & DSMB Ops - Future Opportunities Digital Infuzion is building a pipeline of Regulatory Monitoring & DSMB Operations... ...safety data review workflows (including SAE/AE‑related documentation support) and ensure completeness, quality, and timeliness. Maintain...Flexible hours
- Enterprise Monitoring and Operations | Req#4336 The Enterprise Monitoring and Operations Support Lead is responsible for engineering,... ...monitoring activities ensuring alert escalation procedures, incident documentation within ITSM workflows, and response workflows are executed in...Full timeFlexible hours
$87k - $100k
...patient journey in clinical trials, such as securing sites and recruiting... ...timeframe. Gathers source documents, updates patient files and... ..., informed consent, safety monitoring, etc.) Capable of working independently... ...software developed both in-house and off-the-shelf. Ability to...HouseHourly payTemporary workWork at office- ...solutions provider in Rockville, MD, is hiring an Enterprise Monitoring and Operations Support Lead. This role involves overseeing enterprise... ...proficiency in performance monitoring tools, incident documentation processes, and proactive remediation strategies, while...
- The Emmes Company, LLC is seeking a Medical Officer to provide oversight for clinical trials and ensure medical compliance. The candidate will monitor safety and efficacy data, collaborate with various stakeholders, and provide medical consultancy. With an MD or equivalent...Remote jobFlexible hours
- Security Monitor 3 page is loaded## Security Monitor 3locations: McLean, VAposted on: Posted Todayjob requisition id: R - 100495Position... ...integrity of the base’s security infrastructure.* Track and document all incidents, observations, and activities during assigned shifts...Contract workFor contractorsShift work
$50k - $70k
...Clinical Research Associate (CRA) to support the... ...operational delivery of clinical trials across infectious... ..., including remote monitoring, site communication, and... ...Drive regulatory and document control processes by maintaining... ...sponsor, or site), in-house preferred. Prior...HouseRemote work$120k - $140k
...Details Remote Senior CRA position in the... ...through all phases of the trial. Conducts site visits... ...initiation visits, interim monitoring visits, and close‑out... ...monitors required regulatory documents for study start‑up,... .... Works with in‑house Clinical Trial Assistant...HouseInterim roleLocal areaRemote workFlexible hours$110k - $135k
Responsibilities & Qualifications The Enterprise Monitoring and Operations Support Lead is responsible for overseeing and optimizing... ...assurance (IA) requirements Physical security controls Maintain documentation and evidence to support audit readiness. Documentation &...Full timeContract workTemporary workWork at officeLocal areaMonday to FridayShift workNight shiftWeekend workDay shiftAfternoon shift$62k - $141k
Job Number: R0241424 Continuous Monitoring Analyst The Opportunity Serve as a Continuous Monitoring Analyst responsible for supporting an enterprisewide ongoing authorization program, ensuring systems maintain their Authority to Operate (ATO)/Continuous Authority to Operate...Full timeContract workPart timeWork at officeLocal areaRemote workShift work$89.2k - $147.06k
...of operations. AT&T has an opening for a Consolidated Systems Monitoring Administrator to provide 24x7 monitoring of server and... ...timely work-off. Maintain current and accurate logs, accurately documenting all system outages and pertinent follow-up information as required...Temporary workWork at officeLocal area$110k - $135k
TekSynap is seeking an Enterprise Monitoring and Operations Support Lead in Rockville, MD. In this role, you will oversee and optimize the 24/7/365 monitoring operations within a Network Operations Center (NOC), ensuring rapid incident response and adherence to operational...Night shift- Phase2 Technology is seeking a Continuous Monitoring Analyst in Rockville, Maryland to support an enterprise-wide ongoing authorization program. You will be responsible for ensuring systems maintain their Authority to Operate (ATO) and monitor security controls effectively...
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