Contract, Clinical Trial Associate

The Contract, Clinical Trial Associate provides clinical study and Trial Master File (TMF) support for clinical operations. This includes supporting Clinical Trial Managers (CTMs) with activities related to study start-up, investigator site feasibility and selection, essential document review, and patient enrollment.

Requirements

• Bachelor’s degree in a relevant life science or healthcare-related discipline
• Minimum 2 years of clinical research support experience in a pharmaceutical, biotechnology, or related environment
• Familiarity with clinical trial study documents
• Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines
• Proficiency with Microsoft Word and Excel
• Excellent verbal and written communication and skills
• Ability to work independently and collaboratively in a fast-paced, matrixed team environment
• Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines
• Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects

Benefits

• Competitive hourly salary
• Opportunity to work with a global commercial biopharmaceutical company