Clinical Scientist - Oncology

Syneos Health/ inVentiv Health Commercial LLC; Kentucky; On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (medical, dental, vision)

401(k) company match

Employee Stock Purchase Plan eligibility

Commission and bonus opportunities

Flexible PTO and sick leave

Job summary

Syneos Health/inVentiv Health Commercial LLC is seeking a Clinical Scientist specializing in Oncology. The role focuses on developing medical plans in collaboration with the Medical Director and conducting thorough reviews of medical data.

Responsibilities include managing project scopes, facilitating communication among teams, and ensuring compliance with industry regulations. The position offers competitive benefits including health coverage, 401(k) matching, and flexible paid time off.

Qualifications

• Experience in developing medical plans and coordinating with Medical Directors.
• Ability to analyze medical data and identify risks.
• Familiarity with ICH, GCPs, and privacy guidelines.

Responsibilities

• Develop and oversee medical plans in collaboration with Medical Director.
• Conduct medical reviews and analyze data for risk identification.
• Manage project scope and coordinate with internal teams and vendors.

Job description

Clinical Scientist - Oncology

This role involves collaborating with the Medical Director to develop and oversee medical plans, engaging with external experts, and conducting medical and data reviews.

Job Responsibilities

• Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan) and coordinate acquisition of necessary medical/scientific input.
• Performs regular and ad-hoc medical review of data listings and data visualizations; analyzes data to identify risks and patterns and supports documentation of medical reviews.
• Authors medical data queries, reviews query responses, and approves query closure in association with the Medical Director.
• May assist Medical Director in patient profile review, scientific review of other study-level data, protocol deviation review, and creation of Medical Review Summary reports as needed.
• Partners with Medical Directors for medical data review and safety review meetings, including slide preparation.
• Manages project scope, objectives, and quality of deliverables to ensure project milestones and timelines are met; serves as primary interface between internal team, customers, and vendors in medical data review and eligibility review areas.
• Collaborates with study team members (Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, and Project Management) to identify risks related to data integrity and subject safety, escalating concerns to project leads in a timely manner.
• Attends Trusted Process meetings and may participate in internal and external audits.
• Acquires basic understanding of ongoing protocol designs, disease-related terminology, and pathology.
• Adheres to data privacy guidelines, ICH, GCPs, enterprise policies, SOPs, work instructions, and project plans; also adheres to customer policies and SOPs as required.

Benefits

The benefits for this position may include a company car or car allowance; health benefits (medical, dental, vision); company match 401(k); eligibility to participate in an Employee Stock Purchase Plan; eligibility to earn commissions and bonus based on company and individual performance; and flexible paid time off (PTO) and sick leave.

Salary Range

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education may also be considered so qualifications of incumbents may differ from those listed in the job description. The Company will determine what constitutes equivalent to the qualifications described above. Nothing contained herein should be construed to create an employment contract. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations when appropriate. The Company also complies with the EU Equality Directive and all employment legislation in the countries in which it operates.