Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Syneos Health

Contract Management Assistant, Spanish, Portuguese speaking

Syneos Health

Contract Management Assistant supporting global clinical trial site start-up for Syneos Health, a life sciences services organization. Handling site contracts, regulatory submissions, essential documents, and Trial Master File compliance.

Posted 8/7/2026full-timeRemote • 🇷🇸 SerbiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing Site Start-Up activities, ensuring compliance with regulatory and site contract documentation, and maintaining strong relationships with internal and external stakeholders. Proficient in submitting essential documents to the Trial Master File in accordance with Company SOP and sponsor requirements.

Highest-signal resume keywords
Spanish SpeakingPortuguese SpeakingRegulatory ComplianceSite Contract ManagementClinical Operations Support

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Soft Skills
Relationship BuildingProblem SolvingCollaboration
Tools & Technologies
Trial Master FileCompany SOP
Industry Keywords
Site Start-UpClinical OperationsInvestigator Site ContractsEthics SubmissionsRegulatory Submissions

About the role

Key responsibilities & impact
  • Provide assistance in Site Start-Up activities in investigator site contracts, ethics and regulatory submissions, and essential documents required for site initiation
  • Support global Clinical Operations projects under oversight from the SSU Country Manager and Central and Shared Services leadership
  • Ensure regulatory and site contract documentation complies with sponsor and Company requirements
  • Work with internal and external team members to implement solutions for project and individual site contract problems
  • Establish strong working relationships with customers, internal project teams, and sites
  • Ensure relevant documents are submitted to the Trial Master File according to Company SOP and sponsor requirements

Requirements

What you’ll need
  • Spanish speaking
  • Portuguese speaking
  • Equivalent experience, skills, and/or education will also be considered
  • Ability to support global Clinical Operations projects
  • Ability to ensure regulatory and site contract documentation complies with sponsor and Company requirements
  • Ability to work with internal and external team members on site contract-related problems
  • Ability to establish working relationships with customers, internal project teams, and sites
  • Ability to submit documents to the Trial Master File according to Company SOP and sponsor requirements

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition
  • Total rewards program
  • Inclusive culture
  • Reasonable accommodations, when appropriate