Development Feasibility Mgr

$83,200 - $93,600/Yr

Ampcus - Thousand Oaks, CA

posted 2 months ago

Full-time
Remote - Thousand Oaks, CA
Professional, Scientific, and Technical Services

About the position

Ampcus Inc. is seeking a highly motivated Development Feasibility Manager to join our talented team. This position is fully remote and is based in Thousand Oaks, CA. The Development Feasibility Manager will play a crucial role in maintaining knowledge of the external local clinical trial environment and assessing its impact on study design and execution. The successful candidate will be responsible for developing a repository of Country Landscaping information, known as the Country Site Intelligence Tool, which will support operational delivery by providing insights into site capabilities, performance, regulatory landscape, and treatment patterns. In this role, the Development Feasibility Manager will build both internal and external engagement to identify new investigators and maintain relationships with experts in specific therapy areas. Understanding patient flows and referral pathways will be essential to support global and local operational delivery. The manager will partner with Operational Feasibility Study Managers (OFSMs) and Global Clinical Project Managers (GCPM) representatives to provide local country landscaping data that will be included in program and study design, as well as to inform and support study placement as applicable. Additionally, the Development Feasibility Manager will support site selection within the country or countries to participate in studies based on information gathered through client and site evaluation processes. The role will also involve supporting operating reviews by analyzing client participation and outcomes, predictability, and delivery.

Responsibilities

  • Maintain knowledge of external local clinical trial environment and assess impact on study design and execution.
  • Develop repository of Country Landscaping information (Country Site Intelligence Tool) to support operational delivery.
  • Build internal/external engagement aiming at identifying new investigators and maintaining relationships with experts in specific therapy areas.
  • Understand patient flows and referral pathways in support of global/local operational delivery.
  • Partner with OFSMs and GCPM representatives to provide local country landscaping data for inclusion into the program and study design.
  • Support site selection within the country(ies) to participate in a study based on information gathered through Client and site evaluation process.
  • Support operating reviews by analyzing Client participation and outcomes, predictability and delivery.

Requirements

  • Master's degree, M.D., PharmD and 3 years of experience OR Bachelor's degree and 5 years of experience.
  • BA/BS/BSc OR qualified nurse (RN) OR BA/BS/BSc in life sciences with 5 years in Pharma or biotech.
  • Experience of working in life sciences or medically related field, including biopharmaceutical clinical research experience.

Nice-to-haves

  • Broad work experience in life sciences or medically related field, including biopharmaceutical clinical research experience.
  • Clinical trial management experience.
  • Operational performance experience.
  • International collaboration experience.
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