Associate Project Manager

About the role

Plan, execute, manage, and close clinical trial projects at an award-winning, full-service CRO/Contract Research Organization with over 25 state-of-the-art laboratories across the US, Canada, and China. Core services include drug metabolism, pharmacokinetics/pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Responsibilities

• Manage and monitor project progress and timelines to ensure successful completion.
• Participate and communicate effectively in project meetings with clients on a regular basis as well as with internal departments to ensure projects are met with quality and within the applicable scope and budget.
• Collaborate with the financial sector throughout various stages of projects (invoices and revenue recognition).
• Prepare and review proposals.
• Generate clinical trial-related documentation as needed and per client request.
• Support Management and Business Development teams with new business opportunities.
• Maintain a general working knowledge of phase I-IV clinical trials, FDA regulations/ICH guidelines, and other pertinent regulations.

Requirements

• Associate Degree or higher.
• At least 2-3 years’ experience in a clinical laboratory, CRO, or pharmaceutical environment.
• Previous project management experience.

Skills

• Excellent communication skills.
• Proficient with Excel, Word, PowerPoint, Microsoft Teams, and other computer skills.
• High level of accountability with self and others.
• Hands-on approach with a desire to teach others.
• Track record of challenging the status quo.
• Team and action oriented.
• Problem-solving.
• Able to prioritize workload.

Benefits

• Health and dental insurance.
• 401(k) plan.
• Disability insurance.
• Life insurance.

Location: Exton, PA | Reports to: Senior Project Manager, Central Lab | Full-time