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"