Clinical Research Associate II (CRA II)

San Diego, CA or Remote
Sep 07, 2018
Required Education
Bachelors Degree
Position Type
Full time


Samumed is a pharmaceutical platform company based in San Diego, California, focused on advancing regenerative medicine and oncology applications through research and innovation ( Samumed has discovered new targets and biological processes in the Wnt pathway, allowing the company to develop small molecule drugs that have the potential to address numerous degenerative conditions as well as many forms of cancer. Samumed is currently conducting clinical trials for multiple disease areas, including oncology, osteoarthritis, androgenetic alopecia, psoriasis, degenerative disc disease, and idiopathic pulmonary fibrosis, and it has a broad pipeline targeting areas of significant unmet medical need.

Job Description and Responsibilities:

Samumed is currently looking for a talented and experienced CRA to join its team as a CRA II.  The CRA II participates in the planning, coordination, and monitoring activities of clinical trials in the Clinical Development Department. The CRA II will provide project support in the initiation, execution and close out of assigned clinical studies.  Remote work opens are available for this position.  Primarily responsibilities for the CRA II role include:

  • Providing clinical trial support, including preparation and management of administrative and regulatory documents, and preparation for monitoring visits
  • Completing word processing, spreadsheet and database assignments, including, but not limited to, correspondence, records, reports, scanning, emailing, copying, filing and other tasks
  •  Creating and managing Investigator Site File and ensuring that all documents within the file are complete
  • Creating and maintaining contact lists and supportive documents for Clinical Development Department and for vendors
  • Complying with institutional and departmental policies and procedures
  • Independently monitoring and managing 8-10 clinical sites
  • Co-monitoring/mentoring CRA Is
  • Assisting with vendor management and review of specifications


  • 4 year life sciences or health care related degree
  • Minimum 2 years of experience independent monitoring
  • Proficient in MS Office software
  • Excellent verbal and written communication skills