Demo

Development Feasibility Mgr

ADVANCED BIO-LOGIC SOLUTIONS
Thousand Oaks, CA Full Time
POSTED ON 3/9/2025
AVAILABLE BEFORE 6/9/2025

Description : Note :

  • Open market rate
  • Remote - EST working hours preferred
  • 1 year contract, with possible extension
  • Shift / Schedule - Monday - Fri (flex time zones) 40 hrs a week
  • Not a global role, just supports US

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 (eg, site capabilities, performance, regulatory landscape, treatment patterns etc.)
  • 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 local operational delivery
  • Partner with GFL and GCPM representatives to provide local country landscaping data for inclusion into the program and study design and to inform / support study placement, as applicable
  • Support site selection within the country to participate in a study based on information gathered through FIRE and site evaluation process.
  • Support operating reviews by analyzing FIRE participation and outcomes, predictability and delivery
  • Knowledge

  • Knowledge of local country and international clinical trial management (including regulations & guidelines)
  • Basic Qualifications

  • BA / BS / BSc or qualified nurse (RN)
  • Experience of working in life sciences or medically related field, including biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company, or other relevant clinical setting)
  • Direct feasibility experience with sponsor and / or CRO company
  • Preferred Qualifications
  • BA / BS / BSc in life sciences 5 Pharma or biotech
  • Masters Degree, M.D., PharmD 3 / 1
  • Broad work experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
  • Clinical trial management experience
  • Operational performance experience
  • International collaboration experience
  • Experience with feasibility and site intelligence : Citeline, TriNetX, Study Optimizer, DQS
  • Basic Qualification :

  • Master’s degree and 3 years of experience
  • Bachelor’s degree and 5 years of experience
  • Must Have Skill Sets :

  • Direct Feasibility Experience
  • Landscaping Assessment
  • Intelligence Tool Experience
  • Last time we sourced for this role was many clinical trial managers where they were involved with feasibility but did not have the direct experience with feasibility
  • Scrubbed resume attached (we filled role in 2023 and 2024)
  • Pay Rate  between open rate based on experience.

    This posting is for Contingent Worker, not an FTE"

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