Senior Clinical Research Associate (CRA) Job

CLINICAL RESEARCH ASSOCIATE needed for a ONE (1) YEAR CONTRACT opportunity with Yoh's client located in Wilmington, DE.

The Big Picture - Top Skills Should You Possess:

- Clinical Trials
- Case Report Forms
- Regulatory Documents

What You'll Be Doing:

- Assists in the development and writing of clinical trial documents and manuals, including Case Report Forms, informed consent forms and other regulatory documents
- Participate in the evaluation and selection of investigative sites
- Coordinate and monitor activities at investigational sites; review monitoring trip reports and conduct co-monitoring visits
- Establish study priorities
- Participate in data review and discrepancy resolution
- Monitor study safety
- Ensure study timelines are being met
- Participate in clinical team meetings and trainings
- Serve as a clinical liaison between the Clinical Drug Development Team and other departments
- Undertake special projects on an as needed basis

What You Need to Bring to the Table:

- Three to five years of clinical research experience of which three should be monitoring experience
- Must have working knowledge of Good Clinical Practices and clinical trial processes.
- The ability to manage multiple priorities across several protocols and therapeutic areas simultaneously.

Bonus Points! Otherwise Known As Preferred Qualifications:

- BS/BA degree with strong emphasis on science
- Experience as a Clinical Trial Manager is preferred

WHAT ARE YOU WAITING FOR? APPLY NOW!

RECRUITER: Kara Lloyd

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.

J2W: CLINICAL

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