Lead Clinical Scientist – Oncology, Gynecologic Malignancies

🔥 18 minutes ago

🗽 New York – Remote

🗽 New York – Remote

💵 $67.7k - $115.1k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Work with the Medical Director to develop Medical Management, Medical Data Review, and Eligibility Review Plans • Engage outside experts, consultants, and advisors to obtain medical/scientific input • Perform regular and ad-hoc medical review of data listings and visualizations • Analyze data to identify risks and patterns/trends and document medical reviews • Author medical data queries, review responses, and approve query closure with the Medical Director • Assist with patient profile reviews, scientific study-level data reviews, protocol deviation reviews, and Medical Review Summary reports • Partner with Medical Directors on medical data review and safety review meetings, including slide preparation • Manage project scope, objectives, deliverable quality, milestones, and timelines • Serve as the primary interface among internal teams, customers, and vendors for medical data and eligibility review • Collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management teams • Identify and escalate data integrity, subject safety, project deliverable, and scope concerns • Attend and present at Trusted Process meetings and participate in internal and external audits • Manage a limited number of direct reports and participate in or conduct interviews

🎯 Requirements

• Experience and deep expertise in clinical/medical science and drug development • Basic understanding and knowledge of ongoing protocol designs • Basic understanding of disease-related terminology and pathology • Knowledge of medical data review and eligibility review • Knowledge of data listings and data visualization • Knowledge of data integrity and subject safety risk identification • Familiarity with International Committee on Harmonization (ICH) guidelines • Familiarity with Good Clinical Practices (GCPs) • Adherence to data privacy guidelines, enterprise policies, standard operating procedures, work instructions, and project plans • Equivalent experience, skills, and/or education will be considered

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Company car or car allowance • Medical, Dental and Vision health benefits • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) • Sick time