Clinical Trials Manager

Job description

Our client seeks an experienced and highly motivated individual to join its Clinical Operations team The ideal candidate will focus on assuring requirements of duties to be fulfilled within a team-oriented, fast-paced and cross-disciplinary biotech environment/

Position Overview:
  • Manages overall operation of the entire clinical study including project planning, budget, resource management, contract research organization, and vendor management. 
  • Manages clinical operational plan, and incorporates the study and scientific plan.  Ensures compliance with good clinical practices, and regulatory guidelines. 
  • Recommends and implements innovative process ideas to impact clinical trials management. 
  • Oversees clinical trials staff, CROs, and other vendors and manages all aspects of clinical operational plan. Responsible for managing full scope of study. 
  • Acts as a cross functional liaison to ensure study plan aligns with business development strategies.
Key Responsibilities:
  • Team player, self-motivated and comfortable working in a matrix environment.
  • Able to lead internal and external global, multi-disciplinary teams /CRO study management teams to ensure the successful conduct of clinical trials in accordance with State and Federal regulations, GCP regulations, ICH guidelines, and internal SOPs
  • In depth understanding of GCP
  • Able to prioritize multiple deliverables effectively
  • Author and review as needed clinical study documents (Informed Consent Forms, Clinical Study Plans, Case Report Forms, Statistical Analysis Plan, etc.)
  • Drive IRB/ethics committee and regulatory submissions as needed to support study timelines
  • Effectively evaluate qualified study sites, perform site initiation, plan and present at investigator meetings/advisory boards, and implement study start up activities including development of documents related to conduct of the study in collaboration with the clinical study team Manage and review study budgets and investigator grants
  • Assess study drug requirements and shipment logistics; contribute to labeling strategy
  • Responsible for timelines (from initiation to closure) ensuring they are met
  • Proactively identifies project risks and resolves with some supervision. Much of the above may be delegated to CROs, in which case the candidate should manage the CROs effectively to ensure delivery)
  • B.A./B.S. in a scientific, healthcare or related field. Advanced degree preferred, but not required.
  • Minimum 3 years of clinical trial experience in Pharmaceutical, Biotech or CRO company preferred (Clinical Trial Manager), minimum 5 for a Senior Clinical Trial Manager

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