Senior Manager, Clinical Scientist - Data Review

As a Senior Manager, Clinical Scientist - Data Review at Eikon Therapeutics, you'll support clinical protocol execution by analyzing safety and efficacy data. You'll work closely with various teams to ensure high-quality data review throughout clinical trials, collaborating on protocol development, and contributing to the accurate reporting of results. Your role will involve critical data interpretation and compliance assurance, promoting consistency in data review practices.

Candidates for the Senior Manager, Clinical Scientist - Data Review role at Eikon Therapeutics should have 6+ years of experience along with a post-graduate degree, or 8+ years if holding a bachelor's degree in a relevant scientific field. Prior clinical drug development experience, particularly in oncology, is preferred. The ideal candidate should also be well-versed in clinical research regulatory requirements and should possess strong analytical and communication skills.

To thrive as a Senior Manager, Clinical Scientist - Data Review at Eikon Therapeutics, you should possess strong analytical and critical thinking skills for accurate data interpretation. Excellent communication and collaboration skills are vital, as you'll be coordinating with multiple teams. Additionally, effective time management and the ability to manage competing priorities are necessary to navigate the dynamic environment of clinical trials successfully.

The Senior Manager, Clinical Scientist - Data Review role at Eikon Therapeutics offers substantial growth opportunities. You may have the chance to mentor junior clinical scientists and potentially transition into a Clinical Scientist lead role. Eikon values professional development, encouraging team members to enhance their skills and advance within the organization while contributing to impactful projects.

Eikon Therapeutics offers a comprehensive benefits package for Senior Managers, Clinical Scientists - Data Review, including a generous 401k plan with company matching, extensive medical, dental, and vision insurance coverage, and mental health benefits. Employees also enjoy paid time off, holiday shutdowns, and enhanced parental leave, demonstrating Eikon's commitment to work-life balance and employee well-being.

When answering this question, emphasize your previous roles related to clinical data review, discussing specific projects where your analytical skills were pivotal. Mention tools or methodologies utilized, and how your contributions impacted study outcomes.

Illustrate your understanding of regulations such as GCP and ICH. Discuss approaches you take to stay informed about evolving regulations and how you implement these in your work, demonstrating your proactive attitude towards compliance.

Use the STAR method (Situation, Task, Action, Result) to structure your response. Provide a specific instance that showcases your problem-solving abilities and how your actions led to a positive outcome for the study.

Discuss your planning strategies, perhaps using tools or methodologies that help you. Showcase how you assess project urgency and importance to manage time effectively, and provide examples of successful outcomes due to your organizational skills.

Highlight your collaboration skills by giving examples of successful partnerships in previous roles and stressing the importance of communication, shared goals, and mutual support in achieving successful trial outcomes.

Share your relevant experiences developing protocols and how those protocols support clinical trial objectives. Discuss any cross-functional collaborations and how you ensure alignment with regulatory standards.

List specific tools or software you've worked with, like SAS or R, and provide examples of how you've effectively utilized them for data analysis in clinical trials, which illustrates your technical skills.

Emphasize your openness to constructive criticism, providing a specific instance where feedback enhanced your work. This shows your willingness to learn and improve, essential traits for a Senior Manager.

Discuss your strategies for continuous learning, such as attending webinars, reading industry journals, or participating in professional organizations, which demonstrate your commitment to staying relevant in the field.

Share your perspective on how ensuring data integrity and safety is paramount for clinical trials. Discuss how a thorough review can impact regulatory approvals and patient safety, supporting why you find this role significant.