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Mid Level Pharmaceutical Clinical Trials information

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How much do mid level pharmaceutical clinical trials jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for mid level pharmaceutical clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

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Cities with the most Mid Level Pharmaceutical Clinical Trials job openings:

What are the most commonly searched types of Pharmaceutical Clinical Trials jobs?

The most popular types of Pharmaceutical Clinical Trials jobs are:

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States with the most job openings for Mid Level Pharmaceutical Clinical Trials jobs include:

Mid Level Pharmaceutical Clinical Trials jobs near you
Infographic showing various Mid Level Pharmaceutical Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trials Associate

Bethesda, MD • On-site

TRI Challenge Convention
See more jobs at TRI Challenge Conventionexternal

$36 - $49/hr

Full-time

Posted 5 days ago

Job description

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.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.

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