Clinical Trial Operations Consultant - Medasource : Job Details

Title: Clinical Trial Feasibility/Operations Consultant

Start Date: ASAP

Location: Pleasanton, CA

Contract: 6 months-1 year, M-F (40 hours/week)

The Clinical Trial Feasibility/Operations Consultant will work with a team under direct supervision of the Clinical Trials Operations Manager.

Responsibilities:

• Determine study activities related to clinical trial protocols.
• Work with principal investigators and study teams in clinical trial start up activities.
• Address logistical issues in order to launch clinical trials in medical facilities
• Must demonstrate excellent organizational, interpersonal, and communication skills
• Other duties as required to assist launching clinical trials.

Requirements:

• Bachelor's Degree in related field
• Must demonstrate excellent organizational, interpersonal, and communication skills.
• Experience with implementing/coordinating clinical trials
• Familiarity with medical terminology
• Must be able to work in a Labor/Management Partnership environment.
• Experience with word-processing and spreadsheet software programs

Soft Skills:

• Must be dependable, punctual, detail-oriented, and able to follow detailed protocols precisely.
• Experience with research administration.
• Must be able to work successfully with a wide variety of internal and external project staff and research participants
• Must exhibit a professional manner with a high degree of courtesy, tact, and sensitivity.
• Must be able to work well independently as well as part of a larger multi-disciplinary research team.