Remote Oncology Clinical Scientist — Data & Medical Strategy

Syneos Health, Inc.; Kentucky; Hybrid; USD 90,000 - 120,000; Full time

Benefits offered by this job

Health benefits (Medical)

Dental and Vision

401k match

Employee Stock Purchase Plan

Bonus eligibility

Flexible PTO

Job summary

Syneos Health is a global biopharmaceutical solutions organization. This role partners with Medical Directors to provide clinical and scientific input to early and late-stage clinical development programs, focusing on protocol-specific requirements and ensuring data quality in clinical trials.

Collaborate with study teams to review data, prepare medical reviews, and coordinate input from external experts. The position involves meeting planning, risk assessment, and ensuring compliance with

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 global biopharmaceutical solutions organization. This role partners with Medical Directors to provide clinical and scientific input to early and late-stage clinical development programs, focusing on protocol-specific requirements and ensuring data quality in clinical trials.

Collaborate with study teams to review data, prepare medical reviews, and coordinate input from external experts. The position involves meeting planning, risk assessment, and ensuring compliance with