14 Clinical Trials Associate Jobs in Bethesda, MD
TECHNICAL RESOURCES INT'L is Hiring a Clinical Trials Associate Near Bethesda, MD
- Triage incoming emails, either as HelpDesk or other centralized/group email box.
- Process/track/distribute/upload designated clinical trial documents/artifacts, e.g., protocol deviations, site monitoring visit reports, essential regulatory documents (ERDs), etc. Generate/distribute Monthly/Quarterly reports regarding the documentation to internal and/or external stakeholders.
- Review information in centralized databases, e.g., patient recruitment/accrual, clinical data entered as EDC. Resolve queries, provide analysis assessments, and create/distribute periodic reports to internal and external stakeholders. Participate in centralized monitoring visits (CMVs).
- Provide Meeting/Webinar Support, i.e., distribute invites, track attendance, and complete/distribute meeting minutes/summaries to internal and external parties.
- Adherence to strict project timelines and expectations.
- Troubleshoot issues by applying existing knowledge to solve new problems.
- Create and maintain study specific contact lists.
- Assist with other operational activities when required, including tracking CRA visit schedules and visit statuses, and sending to internal or external stakeholders as directed.
- Reviewing, tracking, and managing study/project documents and filing as appropriate.
- Track progress of tasks and projects.
- Assist CRAs, CSMs, and/or In-House CRAs as needed.
- Knowledge of applicable ICH/GCP/FDA guidelines/regulations in a pharmaceutical, clinical research, or clinical site, sponsor, or CRO setting (i.e., In-house CRA, Study Coordinator, IRB Coordinator, and Regulatory Coordinator/Associate/Specialist).
- Must have excellent time management skills.
- Able to identify activities along critical paths toward a specified deliverable.
- Demonstrated understanding of medical and clinical trials terminology, including general understanding of Clinical Site Monitoring, Essential Regulatory Documents, and Trial Master Files.
- Able to work independently or with minimal supervision and handle multiple tasks effectively while keeping up with rapid changes of priorities without loss of efficiency.
- Demonstrated understanding of sponsor-specific requirements, and Standard Operating Procedures/Project Work Instructions.
- Excellent professional writing and verbal communication skills.
- Must be self-motivated and have a positive attitude.
- Excellent organizational and coordination skills with strong attention to detail.
Job Summary
Full Time
$68k-89k (estimate)
08/05/2023
05/15/2024
The job skills required for Clinical Trials Associate include Clinical Research, Clinical Trial, Standard Operating Procedures, Verbal Communication, Analysis, Coordination, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Trials Associate. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Trials Associate. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Trials Associate positions, which can be used as a reference in future career path planning. As a Clinical Trials Associate, it can be promoted into senior positions as a Clinical Research Associate II that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Trials Associate. You can explore the career advancement for a Clinical Trials Associate below and select your interested title to get hiring information.
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