Clinical Project Manager

Summary

Join Peachtree BioResearch Solutions, a specialized full-service CRO, as a Clinical Project Manager (CPM)! In this role, you will manage clinical studies, drive client relationships, and significantly influence project success. You will collaborate with cross-functional teams, oversee vendors, manage budgets and timelines, and ensure study compliance. The ideal candidate possesses a minimum of 2 years of experience independently managing Phase II or III studies and strong presentation skills. We offer a supportive environment and competitive benefits, including medical, dental, vision, life, and disability coverage, PTO, paid holidays, and a 401(k).

Requirements

• BS or BA degree
• Minimum 2 years of experience independently managing Phase II or III studies with a sponsor or other CRO
• Willingness to work in therapeutic areas that include CNS, Oncology, Cardiometabolic, or Rare Disease
• Superior presentation skills
• Ability to travel occasionally
• Technology: Expert at traditional Business Software and experienced with CTMS and other industry related technology

Responsibilities

• Overall responsibility of project deliverables
• Deep understanding of business factors that can influence the trajectory of projects, and provide guidance to internal and external stakeholders as needed
• Collaborate with Clin Ops, BD, and Finance regarding project specifics and delegate responsibilities accordingly
• Create and manage a cross-functional study team and lead study team members
• Ensure adequate participation, contribution and accountability of the clinical study team members in adherence with applicable SOPs and processes
• Ensure that the study is audit/inspection ready at all times and any resulting findings from audits/inspections are addressed appropriately and in a timely manner
• Vendor oversight including selection, management and quality assurance, especially of monitoring and study management vendors, but also of other area vendors (e.g central laboratories, IVRS, etc), in collaboration with study team members
• Budget management to ensure that the budget appropriately meets the needs of the study, while maintaining cost controls
• Timeline management including the definition, updating and transmittal of the status and planning of the study
• Take on responsibilities as needed across functional areas

Preferred Qualifications

• Therapeutic areas that include CNS, Oncology, Cardiometabolic, or Rare Disease would be beneficial
• Protocol generation of multiple phase II or III clinical study protocols
• Desire to understand the business beyond the project management function - a natural business "curiosity" with a highly positive attitude

Benefits

• Medical, Dental, Vision, Life, Disability coverage
• 20 days PTO + 13 Paid Holidays
• 401(k)