Senior Manager, Clinical Scientist (Contractor)

Eikon Therapeutics is seeking a Clinical Scientist Data Reviewer to support the scientific planning efforts and collaborate with Clinical Research, Pharmacovigilance, and Clinical Operations in the execution of one or more clinical trials. The role will involve analyzing and interpreting clinical trial data to ensure accuracy, integrity, and compliance with regulatory requirements.

Requirements

• 6+ years of experience with a Post Graduate Degree or 8+ years of experience with a Bachelor’s degree in a relevant scientific discipline.
• Experience in clinical drug development experience, or a PhD, Pharm D, or RN degree is preferred.
• Experience within oncology preferred
• Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
• Ability to manage multiple competing priorities with good planning, time management and prioritization skills
• Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions
• Proficient scientific expertise to propose, design, and execute clinical research and development studies, and authors documents related to clinical trials
• Interact with key stakeholders across Clinical Development functional areas
• Role requires proactive approach, strategic thinking and leadership in driving toward clinical study goals
• Influence opinions and decisions of internal and external customers / vendors, across functional areas
• Problem solving, prioritization, conflict resolution and critical thinking skills
• Strong communication, technical writing, and presentation skills experience

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan
• Visa Sponsorship
• Four Day Work Week
• Generous Parental Leave
• Tuition Reimbursement
• Relocation Assistance