Clinical Trial Management Associate (CTMA)

Responsibilities:

• Accountable for study level tracking as assigned by the Clinical Project Manager; e.g. monitor visit tracking and sample tracking.
• Provides study level information to enable accurate and efficient supply of clinical product to the sites.
• Provides regular study updates to the appropriate internal stakeholders.

Qualifications:

• At least 2+ years of relevant experience and a BS or BA in a relevant scientific discipline.
• Relevant clinical trial experience in the pharmaceutical or health care industry or equivalent
• Must be familiar with routine medical/scientific terminology.

Required Skills:

• Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
• Must have working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials
• Team-player with desire to work in a fast-moving, dynamic start-up environment.