IQVIA
Contract Negotiator 1, Clinical Research
Buenos Aires, Argentina
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.6M live jobs from 210,000+ employers in 200+ countries.
Tailor my resume for this job →Apply from your AI assistant
Connect hirly to Claude or ChatGPT and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending.
Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.
hirly's read of this role
- Role family
- Healthcare
- Seniority
- Mid level
- Country
- AR
- Work mode
- On-site / unstated
- First seen by hirly
- 4 Nov 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
We are looking for a Contract Specialist to join our Country Site Activation team!
Location: Argentina - full Home based
- What You´ll Do
- Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Contract negotiations with research sites.
Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.
What Will Help You Succeed
+2 years clinical research experience in contract negotiations with clinical research sites
Health Sciences degree
Advanced command of English language.
Desirable experience in regulatory submissions & imports/exports that correspond to activities subsequent to the authorization of a clinical protocol in the country.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Excellent organization and prioritization skills
Excellent communication and interpersonal skills
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Listed on hirly, a job board. hirly is not the employer: IQVIA is hiring for this role.
Similar jobs
- Clinical Research Associate II - Hematology ( Argentina )Worldwide · Buenos Aires, ArgentinaFirst seen 7d ago
- Clinical Research Associate II - ArgentinaWorldwide · Buenos Aires, ArgentinaFirst seen 10d ago
- FSP Clinical Research Associate IIThermofisher · Remote, ArgentinaFirst seen yesterdayremote
- FSP Clinical Research Associate IThermofisher · Remote, ArgentinaFirst seen 7d agoremote
- Project Specialist with Finance and Clinical Research experience (Home Based Argentina)Syneoshealth · ARG-RemoteFirst seen 27d agoremote
Browse similar roles
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job