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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86 jobs found

Title

Location

Date Posted

Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Clinical Trial Manager with at least 5 years of experience in clinical research and experience as a CTM working with US - Mexico Home Based

Safety & PV Specialist II - Mexico Hybrid

Safety & PV Specialist II - Mexico Hybrid

Safety & PV Specialist I - Mexico Hybrid

Safety & PV Specialist I - Mexico Hybrid

Sr Clinical Trial Manager (Sponsor dedicated) - BA, Argentina with two times per week in client's office

Regulatory Device CMC Manager

Regulatory Device CMC Manager

Principal Clinical Trial Regulatory Affairs - +4 years of experience in regulatory submissions in LATAM - Argentina, Mexico or Brazil Home Based

Principal Clinical Trial Regulatory Affairs - +4 years of experience in regulatory submissions in LATAM - Argentina, Mexico or Brazil Home Based

Site Contracts Specialist (Latam Experience)

IMS Specialist I - Payments Analyst for Clin Trials (Sponsor dedicated) with English advanced - Hybrid, twice a week in Nuñez, Buenos Aires

CRA II FSP

Clinical Site Contracts Specialist - Site agreements & budget experience hybrid BA Argentina

Accountant

CRA II

SSU CRA

Site Contracts Specialist with experience in Clinical Trials, Home-Based Mexico or Brazil

Clinical Trial Manager with focus on project management - Sponsor dedicated - Argentina Home Based

Clinical Data Associate III / Sr CDA (FSP) - Min 2 years of previous data management exp - Argentina, home-based

Strategic Initiatives, Associate Director

Clinical Supply Chain Manager open to several EMEA & LATAM countries (Homebased)

Regulatory Associate - AdPromo

Regulatory Associate - AdPromo

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