Technical Resource Specialist.

JOB PURPOSE:

The Technical Resource Specialist works on all Company clinical trial projects to provide technical expertise to the Project Manager as well as the Client. This person serves as a technical conduit between the Client and the entire MedNet project team.

ESSENTIAL JOB DUTIES:

• Maintain internal Technical coordination and communication for all clinical trials.
• Coordinate cross-functional efforts to achieve study objectives and goals for all clinical trials.
• Review all protocols to match Client Technical needs with appropriate MedNet Services.
• Provide review/comment on case report forms to ensure efficient and thorough approach to website trial architecture. If contracted, develop Client's paper eCRFs for collection of critical data elements as required by the trial protocol.
• Maintains inter- and intradepartmental workflow by fostering a spirit of cooperation.

JOB QUALIFICATIONS:

EDUCATION: Bachelor's Degree.

EXPERIENCE: 2+ years of experience with a medical device, pharmaceutical, CRO or equivalent experience. Candidate must have advanced knowledge of the Microsoft Suite of programs. Advanced database and programming knowledge a requirement as well.

SKILLS AND ABILITIES: Understanding of clinical databases and familiarity with Electronic Data Capture Systems.

To apply for this position, please email your resume and cover letter to humanresources@mednetstudy.com