Syneos Health® (Nasdaq: SYNH) is a leading integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. We support a diverse, equitable and inclusive culture.

Corporate Headquarters

1030 Sync Street
Morrisville, NC 27560

Phone: 919 876 9300
Fax: 919 876 9360
Toll-Free: 866 462 7373

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, including the use of this website, please contact us at: Email: jobs@syneoshealth.com One of our staff members will work with you to provide alternate means to submit your application.

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50 jobs found

Title

Location

Date Posted

Senior Medical Writer (Publication writing)

Medical Writer II (CSR Narrative)

Associate Director, Corporate Quality

Associate Director, QA

Sr Associate, QA

Quality Assurance Associate

Quality Assurance Associate

Quality Assurance Associate

Financial Analyst

Global Compensation Lead

Medical Writer II (Systematic Literature Review (SLR) Writer)

Regulatory Consultant (EU mkt, Module 3)

Principal Professional Quality Risk Manager

Sr Safety & PV Specialist (Literature Review, CP and CAPA Management)

Principal Safety & PV Specialist (Literature CP & Review)

Accounts Receivable Coord I

Accounts Payable Coord I

Accounts Receivable Coord I

Accounts receivable Coord I

Safety & PV Specialist I (Japanese Language)

Senior Regulatory Associate (EU Mkt experience)

Safety & Pharmacovigilance Coordinator (1+ Year Experience in CT or Literature Data Entry)

Associate Director, Change Management

Senior Clinical Programmer (Rave & Veeva CDB Admin URL)

FSP Clinical Scientist

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