Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Development Feasibility Manager
Posted: 03/24/2025
2025-03-24
2025-04-24
Employment Type:
Contract
Job Category: Clinical Development and Operations
Job Number: 618244
Is job remote?: Yes
Country: United States
Job Description
--
Basic Qualification:
Master’s degree and 3 years of experience
OR
Bachelor’s degree and 5 years of experience
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
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, StudyOptimizer, DQS
Knowledge
• Knowledge of local country and international clinical trial management (including regulations & guidelines)
*CO/NYC candidates might not be considered
Basic Qualification:
Master’s degree and 3 years of experience
OR
Bachelor’s degree and 5 years of experience
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
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, StudyOptimizer, DQS
Knowledge
• Knowledge of local country and international clinical trial management (including regulations & guidelines)
*CO/NYC candidates might not be considered
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