Contract Negotiator at IQVIA

Buenos Aires, Buenos Aires, Argentina

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, PharmaceuticalsIndustries

Requirements

+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

Responsibilities

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
Serve as 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
Conduct 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

Skills

Key technologies and capabilities for this role

Contract NegotiationsGCP/ICHRegulatory GuidelinesSite ActivationClinical ResearchSOPsQuality ControlProject ManagementEnglish

Questions & Answers

Common questions about this position

Is this position remote or home-based?

The position is full home based in Argentina.

What experience is required for this Contract Negotiator role?

Candidates need +2 years clinical research experience in contract negotiations with clinical research sites, a Health Sciences degree, and advanced command of English.

What skills are essential to succeed in this role?

Key skills include knowledge and ability to apply GCP/ICH and applicable regulatory guidelines, excellent organization and prioritization skills, and excellent communication and interpersonal skills.

What is the salary or compensation for this position?

This information is not specified in the job description.

What kind of experience will make me stand out as a candidate?

Desirable experience in regulatory submissions & imports/exports related to activities after clinical protocol authorization will help you succeed.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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