Clinical Research Associate

Two CRA positions physically based in Rockville, Maryland. MUST have a minimum two years CRO or pharmaceutical monitoring experience in all phases of clinical trials; MUST be able to travel 50 – 80% of time.

Responsibilities include: identify investigator; conduct pre-study visit; conduct study initiation visits; conduct monitoring visits; prepare reports and letters in accordance with study SOPs; conduct closeout visits; collect, review and process regulatory documents; review SAE’s; maintain investigator files; assists with in-house review of CRFs.

Additional Qualifications: B.S. nursing, pharmacy, or scientific discipline required; MA/MS desirable; variety of therapeutic experience highly desirable; strong organizational skills; the ability to: multi-task, manage multiple study sites and studies; problem-solver and team player; strong written and verbal communication and diplomacy skills; professional demeanor and appearance. 

We offer an excellent benefit package, competitive compensation, and an exceptional, team-oriented work environment. To Be Considered: MUST provide salary requirements and resume to dpjobscra@dpclinical.com or Fax to: 301-294-2233. We are an equal opportunity employer.

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