Clinical/Medical Scientist – Medical Monitoring, Immunology, Dermatology Indications

This is a fully remote position, open to applicants in Alabama, +39 more states.

📋 Description

• Collaborate with the Medical Director to formulate Medical Management, Medical Data Review, and Eligibility Review Plans.

• Engage external experts, consultants, and advisors to gather medical/scientific insights for medical plans.

• Conduct both regular and ad-hoc medical reviews of data listings and visualizations.

• Analyze data to detect risks, patterns, and trends; document findings from medical reviews.

• Identify and resolve issues related to medical data review.

• Create medical data queries, assess responses, and approve query closure with the Medical Director.

• Assist in reviewing patient profiles, scientific study-level data, protocol deviations, and Medical Review Summary reports.

• Collaborate with Medical Directors during medical data review and safety review meetings, including preparing presentation slides.

• Oversee project scope, objectives, deliverable quality, milestones, and timelines.

• Act as the primary liaison among internal teams, customers, and vendors for medical and eligibility review.

• Work with study teams to pinpoint data integrity and subject safety risks.

• Raise project concerns, at-risk deliverables, and out-of-scope tasks to project leads.

• Participate in and present at Trusted Process meetings and engage in audits.

• Comply with data privacy guidelines, ICH, GCPs, enterprise policies, SOPs, work instructions, project plans, and customer requirements.

• Supervise a limited number of direct reports and take part in or conduct interviews.

⛳️ Requirements

• Medical/scientific knowledge pertinent to immunology and dermatology indications.

• Experience in medical data review and eligibility review processes.

• Familiarity with protocol designs, disease-related terminology, and pathology.

• Proficiency in analyzing data listings and visualizations to identify risks and trends.

• Capability to create medical data queries and evaluate query responses.

• Understanding of International Committee on Harmonization (ICH) guidelines and Good Clinical Practices (GCPs).

• Ability to collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management teams.

• Willingness to attend Trusted Process meetings and take part in both internal and external audits.

• Equivalent experience, skills, and/or education may also be considered.

🏝️ Benefits

• Opportunities for career development and advancement.

• Supportive and engaged management.

• Technical and therapeutic area training provided.

• Peer recognition along with a total rewards program.

• An inclusive workplace culture.

• Company car or car allowance available.

• Comprehensive Medical, Dental, and Vision health benefits.

• Company match for 401k contributions.

• Eligibility to participate in the Employee Stock Purchase Plan.

• Opportunity to earn commissions/bonuses based on company and individual performance.

• Flexible paid time off (PTO) policy.

• Paid sick leave.