Clinical Trial Associate


The Clinical Trial Associate provides clinical trial coordination support to the assigned clinical trial or trials. This support includes study deliverable tracking and completion of study documentation including eTMF is maintained for the assigned clinical trial(s). This position will work with internal clinical development team members and with external vendors and CROs. This role may work collaboratively on one program or across several trials to support clinical operations activities.

As a Clinical Trial Associate, you can expect to:

  • Coordinate support trial(s) from start up to close out 
  • Maintain the eTMF with CRO for assigned trials
  • Coordinate and document team meetings 
  • Track and follow up action items for clinical deliverables
  • Reconcile and track purchase orders and invoices 
  • Develop and owe clinical trial tracking documents
  • Ensure trial management documentation is conducted in accordance with ICH/GCP standards
  • Develop and maintain strong, collaborative relationships with multiple cross functional team members
  • Potentially coordinate and track clinical samples

What you'll bring:

  • At least 2 years of trial coordination experience in a clinical research environment, with at least some within the biotech/pharma industry
  • Bachelor’s Degree or higher in a life-science-based subject
  • Basic understanding of drug development
  • Understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies
  • Good verbal and written communication skills

Hemab is an Equal Opportunity and Affirmative Action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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Clinical Trial Associate