Clinical/Medical Scientist – Oncology, Hematology

This is a fully remote position, open to applicants in New York.

📋 Description

• Collaborate with the Medical Director to create medical plans.

• Engage external experts, consultants, and advisors to solicit medical and scientific insights.

• Conduct regular and ad-hoc medical evaluations of data listings and visual representations.

• Analyze data to pinpoint risks and trends, and document the findings of medical reviews.

• Draft medical data queries, assess responses, and finalize query closure in conjunction with the Medical Director.

• Support patient profile assessments, scientific data reviews at the study level, protocol deviation evaluations, and Medical Review Summary reports.

• Collaborate with Medical Directors during medical data evaluations and safety review meetings, including the preparation of presentation slides.

• Oversee project scope, objectives, quality of deliverables, milestones, and timelines.

• Act as the primary liaison among internal teams, clients, and vendors concerning medical data and eligibility assessments.

• Work closely with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management teams.

• Recognize and escalate concerns related to data integrity, subject safety, deliverables, and project scope.

• Participate in and present at Trusted Process meetings and be involved in both internal and external audits.

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

⛳️ Requirements

• Experience in clinical or medical science, particularly in oncology and hematology.

• Capability to formulate medical plans, including the Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan.

• Proven experience in conducting medical reviews of data listings and visual data formats.

• Skill in analyzing data to recognize risks and data patterns or trends.

• Proficiency in drafting medical data queries and evaluating the responses.

• Familiarity with patient profile assessments, study-level scientific data reviews, and protocol deviation evaluations.

• Knowledge of current protocol designs and terminology related to diseases and their pathology.

• Understanding of risks associated with data integrity and subject safety.

• Commitment to adhering to data privacy regulations, ICH guidelines, GCP standards, enterprise policies, SOPs, work instructions, and project plans.

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

🏝️ Benefits

• Opportunities for career development and advancement.

• Supportive and engaged management.

• Training in technical skills and therapeutic areas.

• Recognition from peers and participation in a total rewards program.

• An inclusive workplace culture.

• Company car or car allowance provided.

• Comprehensive medical, dental, and vision benefits.

• 401(k) with company matching.

• Eligibility for the Employee Stock Purchase Plan.

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

• Flexible paid time off (PTO) policy.

• Sick leave available.