The Opportunity

We are looking for a Medical Specialist, working in the Biotechnology/Medical Devices industry in South San Francisco, California, United States.


  • Recruits, schedules, and consents clinical study subjects 
  • Assists in the preparation, handling, distribution, filing, and archiving of clinical study documentation 
  • Accurately maintains Trial Master File documentation to ensure audit readiness 
  • Supports the preparation, handling, tracking, and distribution of Clinical Trial Supplies 
  • Assists with the completion, tracking, and management of Case Report Forms (CRFs), data queries, and clinical data flow 
  • Supports monitoring visits and resolve monitoring findings 
  • Assists Clinical Operations team members with study-related duties as necessary 

The pay range we are offering is 30 to 47 per hour. This position may present an opportunity to go permanent.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success

Minimum Qualifications: 

  • BA/BS degree 
  • 2 years of experience in clinical research 
  • Strong written and verbal communication skills 
  • Effective time management and organizational skills 
  • Attention to detail and accuracy in work 
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients 
  • Computer skills including proficiency in use of Microsoft Word, Excel, PowerPoint and Google Docs 

Preferred Qualifications: 

  • Graduate-level degree or RN 
  • Working knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines 
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.


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