How much does a Senior Clinical Research Associate make in Pennsylvania? The average Senior Clinical Research Associate salary in Pennsylvania is $87,524 as of March 26, 2024, but the range typically falls between $76,204 and $100,255. Salary ranges can vary widely depending on the city and many other important factors, including education, certifications, additional skills, the number of years you have spent in your profession.

Based on HR-reported data: a national average with a geographic differential
Senior Clinical Research Associate Salaries by Percentile
Percentile Salary Location Last Updated
10th Percentile Senior Clinical Research Associate Salary $65,897 PA March 26, 2024
25th Percentile Senior Clinical Research Associate Salary $76,204 PA March 26, 2024
50th Percentile Senior Clinical Research Associate Salary $87,524 PA March 26, 2024
75th Percentile Senior Clinical Research Associate Salary $100,255 PA March 26, 2024
90th Percentile Senior Clinical Research Associate Salary $111,846 PA March 26, 2024
25% $76,204 10% $65,897 90% $111,846 75% $100,255 $87,524 50%(Median) Didn’t find job title? Click
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Check out Senior Clinical Research Associate jobs in Pennsylvania

Senior Clinical Research Associate

Abbott Laboratories - Alameda, CA

Senior Clinical Research Associate

System One Holdings, LLC - Chula Vista, CA

Senior Clinical Research Associate

Research & Development Institute, Inc. - Los Angeles, CA

Senior Clinical Research Associate

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Location Avg. Salary Date Updated
Location Stroudsburg, PA Avg. Salary $88,664 Date Updated March 26, 2024
Location Aaronsburg, PA Avg. Salary $85,069 Date Updated March 26, 2024
Location Abbottstown, PA Avg. Salary $85,419 Date Updated March 26, 2024
Location Abington, PA Avg. Salary $92,523 Date Updated March 26, 2024
Location Ackermanville, PA Avg. Salary $92,172 Date Updated March 26, 2024
Location Acme, PA Avg. Salary $81,911 Date Updated March 26, 2024
Location Acosta, PA Avg. Salary $78,754 Date Updated March 26, 2024
Location Adah, PA Avg. Salary $85,858 Date Updated March 26, 2024
Location Adamsburg, PA Avg. Salary $86,033 Date Updated March 26, 2024
Location Adamstown, PA Avg. Salary $87,261 Date Updated March 26, 2024
Job Openings for Senior Clinical Research Associate in Pennsylvania
THE COMPANY 89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product candidate, pegozafermin (BIO89-100), is a specifically engineered glycoPEGylated analog of FGF21. Pegozafermin is being developed for the treatment of nonalcoholic steatohepatitis (NASH) and severe hypertriglyceridemia (SHTG). THE ROLE The In-House Clinical Research Associate/Senior Clinical Research Associate will participate in planning and assisting in overseeing the conduct of clinical trials in accordance with Company policies and procedures and applicable regulations. THE RESPONSIBILITIES Participate in all aspects of assigned clinical studies to ensure studies are completed on time, within budget, and in compliance with FDA regulations and ICH/GCP guidelines. Participate in the design and development of clinical trial protocols and case report forms. Contribute
- 2 days ago
Bayside Solutions - Kansas City , KS
Senior Clinical Research Associate Direct Hire Fulltime Role Salary Range: $120,000 - $140,000 per year Location: US Central - Remote with Travel Job Summary: As a Senior Clinical Research Associate, you will be integral in successfully monitoring and managing clinical trials. The responsibilities of a Senior CRA include ensuring clinical trials are conducted, recorded, and reported following protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. This role will require frequent travel up to 65% of the time. Duties and Responsibilities: Monitor clinical studies of investigational and approved products that satisfy a medical need or offer a commercial benefit, including site visits for qualification, initiation, interim, and close-out Manage and train site personnel on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. Manage and track the preparation and return of investigational supplies
- 2 days ago
Bayside Solutions - Kansas City , MO
Senior Clinical Research Associate Direct Hire Fulltime Role Salary Range: $120,000 - $140,000 per year Location: US Central - Remote with Travel Job Summary: As a Senior Clinical Research Associate, you will be integral in successfully monitoring and managing clinical trials. The responsibilities of a Senior CRA include ensuring clinical trials are conducted, recorded, and reported following protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. This role will require frequent travel up to 65% of the time. Duties and Responsibilities: Monitor clinical studies of investigational and approved products that satisfy a medical need or offer a commercial benefit, including site visits for qualification, initiation, interim, and close-out Manage and train site personnel on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. Manage and track the preparation and return of investigational supplies
- 2 days ago
THE COMPANY 89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product candidate, pegozafermin (BIO89-100), is a specifically engineered glycoPEGylated analog of FGF21. Pegozafermin is being developed for the treatment of nonalcoholic steatohepatitis (NASH) and severe hypertriglyceridemia (SHTG). THE ROLE The In-HouseClinical Research Associate/Senior Clinical Research Associate will participate in planning and assisting in overseeing the conduct of clinical trials in accordance with Company policies and procedures and applicable regulations. THE RESPONSIBILITIES Participate in all aspects of assigned clinical studies to ensure studies are completed on time, within budget, and in compliance with FDA regulations and ICH/GCP guidelines. Participate in the design and development of clinical trial protocols and case report forms. Contribute
- 3 days ago
Bayside Solutions - Kansas City , MO
Senior Clinical Research Associate Direct Hire Fulltime Role Salary Range: $120,000 - $140,000 per year Location: US Central - Remote with Travel Job Summary: As a Senior Clinical Research Associate, you will be integral in successfully monitoring and managing clinical trials. The responsibilities of a Senior CRA include ensuring clinical trials are conducted, recorded, and reported following protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. This role will require frequent travel up to 65% of the time. Duties and Responsibilities: Monitor clinical studies of investigational and approved products that satisfy a medical need or offer a commercial benefit, including site visits for qualification, initiation, interim, and close-out Manage and train site personnel on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. Manage and track the preparation and return of investigational supplies
- 3 days ago
Bayside Solutions - Kansas City , KS
Senior Clinical Research Associate Direct Hire Fulltime Role Salary Range: $120,000 - $140,000 per year Location: US Central - Remote with Travel Job Summary: As a Senior Clinical Research Associate, you will be integral in successfully monitoring and managing clinical trials. The responsibilities of a Senior CRA include ensuring clinical trials are conducted, recorded, and reported following protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. This role will require frequent travel up to 65% of the time. Duties and Responsibilities: Monitor clinical studies of investigational and approved products that satisfy a medical need or offer a commercial benefit, including site visits for qualification, initiation, interim, and close-out Manage and train site personnel on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. Manage and track the preparation and return of investigational supplies
- 3 days ago

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