Clinical Research Associate Specialist

4 days ago


King of Prussia, Pennsylvania, United States Parexel International Corporation Full time

Are you looking for a challenging role in clinical research? We are seeking an experienced Clinical Research Associate I to join our team at Parexel International Corporation. As a key member of our study start up team, you will be responsible for managing and driving the strategy for Pre SIV / start up tasks of clinical trials.

In this role, you will participate in pre-initiation activities, build relationships with investigators and site staff, and generate visit/contact reports. You will also develop strategies to configure, distribute, and collect high-quality country-specific and/or site-specific documents or essential regulatory documents (SRP).

You will have the opportunity to customize, review, and negotiate country/site-specific Informed Consent Forms (ICF), translations, and amendments. Additionally, you will prepare and submit IRB/IEC and MoH/RA application(s) and resolve conflicts until receipt of final approval.

This is a unique opportunity to work with a leading Contract Research Organization (CRO) like Parexel International Corporation. With a strong focus on client satisfaction, we offer a dynamic and challenging work environment that fosters growth and development.

The salary for this position is estimated to be around $65,000 - $80,000 per year, depending on location and experience. If you are a motivated and detail-oriented individual with excellent communication skills, we encourage you to apply.

Job Responsibilities
  • Manage and drive the strategy for Pre SIV / start up tasks of clinical trials
  • Participate in pre-initiation activities
  • Build relationships with investigators and site staff
  • Generate visit/contact reports
  • Develop strategies to configure, distribute, and collect high-quality country-specific and/or site-specific documents or essential regulatory documents (SRP)
  • Customize, review, and negotiate country/site-specific Informed Consent Forms (ICF), translations, and amendments
  • Prepare and submit IRB/IEC and MoH/RA application(s) and resolve conflicts until receipt of final approval

We offer a competitive compensation package, including benefits and opportunities for career growth and development. Apply now to become part of our team


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