Eikon Therapeutics is seeking a Senior Manager, Clinical Scientist Data Reviewer to support scientific planning efforts and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of clinical trials. The role involves 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
- 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
- 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
- 401k plan with company matching
- Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
- Mental health and wellness benefits
- Weeklong summer and winter holiday shutdowns
- Generous paid time off and holiday policies
- Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
- Enhanced parental leave benefit
- Daily subsidized lunch program when on-site
