Clinical Research Coordinator

US$40 - US$50 per hour + Highly Competitive Salary
  1. Contract
  2. Project/Study Manager (CSM/CPM), Program Manager / Director, Clinical Scientist
  3. United States
San Francisco, USA
Posting date: 11 Mar 2024

This vacancy has now expired. Please see similar roles below...

Clinical Research Coordinator - Contract - Onsite

Proclinical Staffing is seeking a Clinical Research Coordinator to join a cutting-edge research institute. This is a contract role located in San Francisco, CA.

Primary Responsibilities

As Clinical Research Coordinator, you will be an essential member of our clinical team, responsible for all aspects of clinical research, from study start-up to close-out.

Skills & Requirements:

  • B.A./B.S. degree (or equivalent combination of education and experience) in Health-related field
  • Clinical Research: 1 year (Required)
  • Administrative: 1 year (Preferred)
  • Business development: 1 year (Preferred)
  • Phlebotomy license (Preferred)

The Clinical Research Coordinator will:

  • Coordinate, monitor, and supervise all aspects of clinical studies from start-up to closeout, to ensure proper execution of assigned clinical research trials and to ensure that study protocols are met
  • Coordinate studies, staff, and relationships in multiple specialty clinics and hospitals
  • Facilitate pre-study activities, including NDA, regulatory documents, IRB submissions, CTA and budget negotiation, and leading SQVs and SIVs
  • Responsible for recruiting and screening patients and scheduling appointments, recruit patients to fill pharma studies in a timely manner
  • Obtain vital signs (i.e., blood pressure, temperature, heart rate, waist measurement, weight & height), perform blood draws, assist with urine and stool collection, use ECG/EKG, prepare, package, and ship specimen
  • Prepare and maintain administrative logs and trackers, including Regulatory Documents Collection tracker, eTMF tracker, Central IRB Submission tracker, Site Shipments tracker, study visits, etc.
  • Fill and track study visits, survey documents, including monitoring reports and study source documents
  • Data Entry to EDC system
  • Answer Sponsor queries, communicate with Sponsor, CROs, PIs, staff members
  • Other duties as assigned by supervising Clinical Research Coordinator or management

If you are having difficulty in applying or if you have any questions, please contact Bodin Forsen at (+1) 617-830-1769 or

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.