Senior Manager, Clinical Scientist

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.

Position

We are seeking a Clinical Scientist Data Reviewer that will support the scientific planning efforts and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate technical skills and scientific acumen as part of a cross-functional clinical development team. You will be a key contributor and supporter in the clinical science activities of evidence generation for regulatory approval and/or engagement with physicians, including protocol development, study implementation, data analysis and reporting of results. This role will be focused on the detailed and critical safety data review efforts from study start-up through final CSR. The Clinical Scientist Data Reviewer is a crucial role in analyzing and interpreting clinical trial data to ensure accuracy, integrity, and compliance with regulatory requirements. There is additional room for growth and leadership opportunities in this role.

This is a contract role, expected to last approximately 6 months, with an anticipated workload of 40 hours per week.

About You

You are a data driven and collaborative integrator that is passionate about driving development and execution of therapeutic strategies that enable innovative pipeline impact and delivery of transformative medicines to patients. You have exemplary communication and presentation skills and can support study development by applying the most current electronic document conventions/processes consistently to ensure scientific and data integrity.

What You'll Do

Responsible for supporting specific aspects of clinical/scientific execution of clinical protocol(s). This may include:

• Serving as a supportive clinical scientist data reviewer focused on safety, efficacy and critical data deliveries as part of the clinical trial team
• Supporting the clinical study team as part of the clinical sciences functional line which is closely aligned with the medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with Clinical Research and Pharmacovigilance (as well as other functional areas in this matrix environment)
• Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); partnering with Clinical Operations on critical and key study deliverables
• Ensure CRF design supports data collection in alignment with the Protocol in collaboration with Clinical Data Management/Programming
• Collaborating cross-functionally to review clinical data to ensure quality, completeness, and integrity of trial conduct
• Potential to provide tactical/scientific mentorship to other clinical scientists and move into Clinical Scientist lead role as well as focus on scientific growth and development
• Responsible for assisting with the generation, analysis, and presentation of clinical data, including manuscripts, abstracts, and oral presentations (including authoring documents and slide preparation as appropriate)
• Apply proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; identifies risks and designs mitigation strategies
• Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs

Qualifications

• 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, such as medical monitoring plan, SAPs, informed consent and clinical components of the Clinical Study Reports
• 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

The expected hourly range for this role is $78.36 to $85.86 depending on skills, competency, and the market demand for your expertise.

Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.

We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.

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