
Senior Clinical Site Manager
1 week ago
Site Acquisition Specialist
This role is a vital component of our team, responsible for leading the site selection process from feasibility assessment to contract negotiation. The ideal candidate will have a strong understanding of clinical trial processes, including site selection and feasibility assessments.
Key Responsibilities:- Feasibility Process Management: Oversee the entire feasibility and site identification process, ensuring alignment with program or protocol requirements.
- Collaboration: Collaborate with cross-functional teams to collect feedback from sites and investigators in the pre-award phase, summarizing and analyzing results.
- Site Profile Evaluation: Evaluate potential site sources, considering their advantages and disadvantages.
- Timeline Target Site Management: Manage timelines and track changes to target site list requirements.
- Survey Creation Data Accuracy: Ensure the accuracy and quality of survey-driven data.
- Literature and Internet Searches: Conduct necessary literature and internet research to support site identification efforts.
- Risk Identification Contingency Planning: Identify potential risks and discuss contingency plans with stakeholders.
- Education: Bachelor's degree in life sciences, business, or related field, or equivalent combination of education and experience.
- Experience: Proven experience in feasibility, site identification, or clinical research, preferably within a CRO or pharmaceutical/biotech setting.
- Strong Analytical Skills: Ability to analyze and interpret data, with a focus on quality and accuracy.
- Excellent Communication Skills: Strong collaboration skills and ability to manage multiple stakeholders.
- Competitive Salary: Based on skills and experience.
- Comprehensive Benefits Package: Including health insurance, life insurance, 401(k) plan, paid time off, employee stock purchase plan, and company bonus.
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