Remote Oncology Clinical Scientist

Syneos Health, Inc.; North Carolina; Hybrid; USD 110,000 - 165,000; Full time

Benefits offered by this job

Health benefits

Company car or car allowance

401k with company match

Paid time off

Job summary

Syneos Health is a leading fully integrated biopharmaceutical solutions organization. This Clinical Scientist - Oncology role supports medical data review, protocol-specific requirements, and data integrity across clinical trials.

You will collaborate with Medical Directors and cross-functional teams to ensure scientific rigor, manage data reviews and safety discussions, and contribute to timely delivery of therapies.

Responsibilities

• Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans.
• Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews.
• Authors medical data queries and reviews query responses, approves query closure in association with Medical Director.
• May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed.
• Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed.
• Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review.
• Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out-of-scope tasks to the project leads in a timely manner.
• Attends at Trusted Process meetings and may participate in internal and external audits.
• Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology.
• Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans.

Job description

Syneos Health is a leading fully integrated biopharmaceutical solutions organization. This Clinical Scientist - Oncology role supports medical data review, protocol-specific requirements, and data integrity across clinical trials.

You will collaborate with Medical Directors and cross-functional teams to ensure scientific rigor, manage data reviews and safety discussions, and contribute to timely delivery of therapies.