[Hiring] Clinical Trial Manager @Parexel

Role Description

The Clinical Trial Manager is responsible for the execution of study-level activities including but not limited to:

• Creating and updating trial-specific documents
• Vendor oversight & delivery
• Compound training
• Country and regional oversight of CRO operational delivery

This includes alignment on the feasibility strategy, target setting, risk reviews, and country challenges that could impact overall study delivery.

Qualifications

• Minimum 5+ years of clinical research experience gained with a CRO, biotech or pharmaceutical company working on phase I-IV global clinical trials
• 2-3 years leading aspects of global clinical trials
• Experience working with CROs
• Bachelor's degree is required

Requirements

• Excellent decision-making, analytical, and financial management skills
• Excellent leadership skills, proven ability to foster team productivity and cohesiveness
• Ability to operate and execute with limited supervision
• Experience in leading without authority in multifunctional matrixed and global environments
• Experience mentoring and coaching others
• Exceptional organizational skills and ability to deal with competing priorities
• Strong reasoning and problem-solving abilities
• Strong project planning/management, communications (written and verbal) and presentation skills
• Experience with protocol, informed consent form (ICF), case report form (CRF), and clinical study report (CSR) development and review
• Proficient in MS Office Suite (Excel, Word, and PowerPoint)
• Ability to travel approximately 10%

Company Description

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.