US Feasibility Manager

job summary: Join a top-tier leader as a US Feasibility Manager. This role offers the flexibility of being 100% Remote (must work EST hours) or based in Ridgefield, CT. You will play a critical role in shaping clinical trial success by driving site identification and outreach strategies across diverse therapeutic programs.

location:

Ridgefield, Connecticut job type: Contract salary: $55.00 - 57.86 per hour work hours: 9 to 5 education: Bachelors responsibilities: Develop and deploy comprehensive country and site feasibility assessments for US-based clinical trials. Identify and vet highly capable investigators and sites to ensure study requirements and business objectives are met. Provide quality feasibility outputs by serving as a subject matter expert on clinical systems and databases. Align with internal stakeholders to ensure recommendations are tactically feasible from a holistic industry perspective. Evaluate scientific literature and data to qualify sites and staff for Phase I-IV clinical human trials.

qualifications:

Required:

Bachelor's Degree in Life Sciences, Pharmacy, or a Nursing Diploma (RN). Minimum of 4 years of experience in the regulated pharmaceutical, CRO, or healthcare industry. Proven experience in site identification, outreach, and managing regional/local feasibilities. Advanced understanding of

FDA/ICH GCP

regulations and IND/NDA federal requirements. Proficiency in clinical trial phases (I-IV) and sponsor qualification criteria.

Preferred:

Background as a Clinical Research Coordinator, Clinical Monitor, or Site Manager. Advanced degree (MS or PhD). #LI-HK1 skills: Phase I, Phase II, Phase iii, Phase iv, Good Clinical Practice (GCP), International Council for Harmonization (ICH)

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. job detailssummary$55 - $57.86 per hourcontractbachelor degreecategorylife, physical, and social science occupationsreference53593job details job summary: Join a top-tier leader as a US Feasibility Manager. This role offers the flexibility of being 100% Remote (must work EST hours) or based in Ridgefield, CT. You will play a critical role in shaping clinical trial success by driving site identification and outreach strategies across diverse therapeutic programs.

location:

Ridgefield, Connecticut job type: Contract salary: $55.00 - 57.86 per hour work hours: 9 to 5 education: Bachelors responsibilities: Develop and deploy comprehensive country and site feasibility assessments for US-based clinical trials. Identify and vet highly capable investigators and sites to ensure study requirements and business objectives are met. Provide quality feasibility outputs by serving as a subject matter expert on clinical systems and databases. Align with internal stakeholders to ensure recommendations are tactically feasible from a holistic industry perspective. Evaluate scientific literature and data to qualify sites and staff for Phase I-IV clinical human trials.

qualifications:

Required:

Bachelor's Degree in Life Sciences, Pharmacy, or a Nursing Diploma (RN). Minimum of 4 years of experience in the regulated pharmaceutical, CRO, or healthcare industry. Proven experience in site identification, outreach, and managing regional/local feasibilities. Advanced understanding of

FDA/ICH GCP

regulations and IND/NDA federal requirements. Proficiency in clinical trial phases (I-IV) and sponsor qualification criteria.

Preferred:

Background as a Clinical Research Coordinator, Clinical Monitor, or Site Manager. Advanced degree (MS or PhD). #LI-HK1 skills: Phase I, Phase II, Phase iii, Phase iv, Good Clinical Practice (GCP), International Council for Harmonization (ICH)

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.