Clinical Scientist - Respiratory

Syneos Health, Inc.; Morrisville (NC); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health benefits (medical, dental, vision)

401(k) match

Flexible paid time off (PTO)

Job summary

Syneos Health, Inc. is seeking a Clinical Scientist in Morrisville, NC. This role involves partnering with Medical Directors to ensure scientific integrity in clinical development programs.

The ideal candidate will manage medical reviews, collaborate with multiple teams, and uphold data integrity throughout clinical trials. Benefits include health coverage, a company car or allowance, and a 401(k) matching program.

Qualifications

• Experience in clinical research or biopharmaceuticals.
• Understanding of ICH, GCP guidelines, and medical data management.
• Strong analytical skills and attention to detail.

Responsibilities

• Develop medical plans with Medical Directors.
• Conduct medical reviews of data listings.
• Manage project scope and quality of deliverables.

Skills

Medical Data Review

Data Analysis

Project Management

Collaboration

Education

Degree in Life Sciences or related field

Job description

Updated: Yesterday

Location: Morrisville, NC, United States

Job ID: 25108957-OTHLOC-1500-2DIN-2DR

Job Title: Clinical Scientist – Respiratory

Overview

Syneos Health® is a biopharmaceutical solutions organization that integrates clinical, medical affairs and commercial insights to accelerate the delivery of therapies.

Key Responsibilities

• Work with the Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engage outside experts, consultants and advisors to obtain necessary medical/scientific input.
• Perform regular and ad‑hoc medical reviews of data listings and visualizations; analyze data to identify risks, patterns and trends; support documentation of medical reviews.
• Author medical data queries, review responses, and approve query closure in collaboration with the Medical Director.
• Assist in patient profile reviews, scientific reviews of study‑level data, protocol deviation reviews, and creation of Medical Review Summary reports.
• Partner with Medical Directors for medical data review and safety review meetings, including slide preparation as needed.
• Manage project scope, objectives, and quality of deliverables to meet milestones and timelines; serve as primary interface between internal team, customers, and vendors for medical data and eligibility review.
• Collaborate with study team members (Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, Project Management) to identify risks related to data integrity and subject safety; elevate project concerns to the appropriate leads.
• Attend Trusted Process meetings and participate in internal and external audits.
• Acquire a basic understanding of protocol designs, disease terminology and pathology.
• Adhere to data privacy guidelines, ICH, GCP, enterprise policies, SOPs, work instructions, and project plans; comply with customer policies as required.

Benefits

This position may include a company car or car allowance, health benefits (medical, dental, vision), company match 401(k), eligibility to participate in the Employee Stock Purchase Plan, commissions/bonus based on performance, and flexible paid time off (PTO) and sick leave. Eligibility for paid sick time may vary by location. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

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 candidate qualifications, skills, competencies, and proficiency for the role.

Summary

Partner with Medical Directors to provide clinical and scientific input to early and late‑stage clinical development programs. Ensure scientific integrity and data quality of clinical trials through protocol‑specific requirements and collaborative data reviews.

Additional Information

Tasks, duties, and responsibilities listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, or job responsibilities. Equivalent experience, skills, and/or education will also be considered. Nothing herein constitutes an employment contract. This description complies with all applicable employment laws and the EU Equality Directive; the Company is committed to compliance with the Americans with Disabilities Act, providing reasonable accommodations as needed.