Clinical Project Manager

17 Nov 2024

Vacancy expired!

Job Description

· Responsible for design, oversight and conduct of the clinical research programs and clinical trials cross functionally from start to close out

· Represent Clinical Operations as a core team member across applicable cross functional team meeting

· Develop clinical program and/or study execution timelines and provide status updates to senior management via governance channels

· Manage the overall program and/or study budgets and track progress against the approved budget and financials

· Lead and oversee development of the study documentation while managing high quality standards in line with applicable SOPs and regulatory requirements

· Lead and manage the process for the selection, contracting and oversight of CROs and/or clinical trial related third party vendors in collaboration with the study team and key stakeholders

· Provide oversight and input, as needed, to development and maintenance of the Study Project Plans including, but not limited to, site selection and monitoring plans, TMF management plan, site payment plans, etc.

· Participate in development and/or improvement efforts within clinical operations including but not limited to best practices and SOPs development

· Evaluate and identify resourcing needs and continuously monitor resourcing over the life cycle of the program and/or study

· Manage training and oversight of the Clinical Operations and/or Clinical Study Teams as assigned

Qualifications

· Bachelor’s degree required (scientific or healthcare discipline preferred) and advanced degree (e.g. Master, PharmD, PhD) preferred

· At least >7 years of clinical research experience with at least 3-5 years of experience in managing and leading clinical program and/or clinical trials

· Experience in working with different systems such as CTMS, EDC, eTMF, IVRS

· Proficiency in web-based systems and project management applications (eg. Microsoft Office, SharePoint, etc.)

· Being able to follow and comply with assigned SOPs

· Knowledge of ICH-GCP and applicable regulatory agency regulations

· Effective communication, interpersonal and leadership skills with ability to partner with cross functional internal and external stakeholders

· Must be able to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and procedures.

· Ability to develop tools and processes that increase measured efficiencies of the project

· Must be able to anticipate obstacles and proactively develop solutions to achieve project goals

· Experience managing/mentoring and developing junior staff

· Demonstrated experience in change management initiatives

Additional Information

All candidates must be legally eligible to work in the United States.

We are an equal opportunity employer. M/F/D/V

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.

  • ID: #22937173
  • State: Kansas Overlandpark 66204 Overlandpark USA
  • City: Overlandpark
  • Salary: USD TBD TBD
  • Job type: Full-time
  • Showed: 2021-11-17
  • Deadline: 2022-01-16
  • Category: Et cetera