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Job Details

Senior Clinical Research Associate/Biopharma

Company: Chiltern
Location: Mid-West or West Coast in the United States
Reference: 0001
Closing Date: 20 Aug 18
Type: Full Time
Salary (£): On Application
Benefits: Excellent and competitive benefits

Job Summary:

Performs study-related tasks as required by the Department.


Job Background

Why be a CRA for Chiltern?

  • Your input is valued, you are not just a number here!
  • Competitive benefits

In this role, the SCRA is responsible for the timely production of high quality data, adhering to the standards set by the Company/Sponsor in the Standard Operating Procedures for clinical studies. The SCRA, in concert with the Project Leader, is accountable for the timely, quality, satisfactory, and cost-effective completion of the client's study.

  • Identifies potential investigational sites
  • Coordinates and performs comprehensive site management, including ISF/TMF maintenance and site correspondence
  • Conducts pre-study, initiation, interim and close out monitoring visits
  • Produces comprehensive visit, status and telephone contact reports
  • Resolves data issues and audit issues
  • Adheres to study timelines and budget
  • Mentors other CRAs
  • Collects high quality essential documents and supports completion of ethics committee and regulatory submissions (if applicable per region)

Bachelor's degree and at least five years of experience as a Senior Clinical Research Associate working with Ophthalmology - Back of the eye, Endocrinology, NASH - liver diseases, Musculoskeletal - Rheumatoid Arthritis.

Chiltern is an EEO / AA Employer and is committed to providing opportunities to minorities, women, individuals with disabilities and veterans.



Position Type

Full Time


Email Michelle Moldavan -
+1 484 679 2491

Apply for this job: Senior Clinical Research Associate/Biopharma

Contact Information:

Address:  Pennsylvania, USA
1016 W 9th Ave, King of Prussia, United States
PA 19406
Website:  Visit Our Web Site

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