Site Contract Specialist

IQVIA; São Paulo; Presencial; BRL 120.000 - 150.000; Tempo integral

Resumo da oferta

A global provider of clinical research services is seeking a SITE CONTRACT SPECIALIST in São Paulo, Brazil. The role involves preparing, negotiating, and finalizing agreements related to clinical trials. Candidates must have a Bachelor’s degree and 5 years of experience in the legal or pharmaceutical industry. Strong negotiation and analytical skills are essential. This position offers the opportunity to work with global teams to enhance clinical research efforts.

Qualificações

• 5 years' experience in the legal/pharmaceutical industry or clinical research.
• Working knowledge of the clinical development process.
• Experience in negotiation and contract management.

Responsabilidades

• Prepare, negotiate, and finalize clinical trial agreements.
• Work with global teams on contractual terms.
• Manage the contract amendment lifecycle.

Conhecimentos

Negotiation skills

Contract management

Analytical thinking

Formação académica

Bachelor’s degree in scientific or business disciplines

Descrição da oferta de emprego

SITE CONTRACT SPECIALIST

Prepare, negotiate and finalize agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations.

Provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts.

Deliverables:

• Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversight of a Clinical Research Organization responsible for contract negotiations.
• Responsible for delivery on established targets/measurements.
• Work with global teams to review and analyze contractual terms and conditions. Assess legal and budget risks in conjunction with team support functions. Partner with Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and drive resolution. Escalate as appropriate.
• Analyze investigator fees in relation to fair market value pricing and ensure alignment with regional standards and the Sponsor pricing guidelines. Participate in and/or lead approval escalations as appropriate.
• Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required.
• Participate in discussions related to the development of site/investigator budgets aligned with fair market value.
• Manage the contract amendment lifecycle.

Education and Experience Requirements:

• Bachelor’s degree in appropriate scientific or business disciplines.
• 5 years’ experience and/or equivalent competencies in legal/ pharmaceutical industry/clinical research.
• Working knowledge of the clinical development process with two (2) years of negotiation and contract experience.
• Accomplish substantial tasks with minimal supervision.
• Previous experience working in virtual teams.

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