Specialist, Site Contracts- Argentina / Brazil

Worldwide; Buenos Aires; Híbrido; ARS 90.547.000 - 135.820.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Specialist, Site Contracts to draft, negotiate, and finalize site agreements and amendments. You will review budgets, coordinate translations, and escalate risks with internal teams to ensure compliant, timely contract execution. Strong English, contract management software proficiency, and ability to manage multiple sites are essential. This role offers remote work with international scope.

Formación

• Bachelor’s degree or equivalent in business, finance, science, or related field.
• 1–3 years in CRO/pharma/clinical research with investigator/site contracts or related legal field.
• Excellent English written and verbal communication skills.

Responsabilidades

• Prepare country contract templates and site agreements.
• Negotiate contract language and budgets with sites to finalization/execution.
• Coordinate with legal, regulatory, and study teams for submission and sign-off.
• Maintain tracking tools for contract lifecycle and timelines.
• Facilitate contract signatures and distribution to sites and sponsor.

Conocimientos

Contract negotiation

Regulatory compliance

Communication

Collaboration

Technical proficiency

Problem solving

Time management

Educación

Bachelor’s degree or equivalent in business/admin, finance, science, or related field

Herramientas

Contract management software

Microsoft Word

Excel

Descripción del empleo

## Specialist, Site ContractsApply: Remote: Buenos Aires, Argentina: Brasilia, Brazil: Full time: Posted Yesterday: JR102935**Who we are**We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.**Why Worldwide**We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!**What the Specialist, Site Contract does at Worldwide**The Specialist, Site Contracts is responsible for the development, preparation, negotiation, and finalization, or assistance in preparation, negotiation, and finalization, of Site Agreements, amendments, or any other document associated between sponsors and clinical research sites**What you will do*** Prepare country contract templates* Draft and send Site Agreements or any contracts associated with sites to begin negotiations* Provide site contract execution planned timelines and site negotiation status* Send items for translation, if applicable, and receive and translate items* Review study budgets and costs pertaining to contract negotiation* Negotiate contract language and budgets with each assigned site to finalization/execution* Escalate site requests outside of preapproved parameters to the Site Contracts Lead for forwarding to the Sponsor* Escalate risks and non-responsive sites to the Site Contracts Lead or internal team, as applicable* Ensure appropriate information or appendices are added to Site Agreements or related documents when equipment is provided to sites* Create donation agreements, as applicable* Review Site Agreements or associated contracts for completeness and accuracy* Finalize contracts and budgets with sites* Perform quality checks of Site Agreements or associated documents before the signature process begins* Provide draft or signed contracts and budgets to the regulatory team for submission purposes when requested* Liaise with Worldwide Clinical Trials Legal Department, Data Privacy team, study teams, Sponsors, sites, investigators, and others as needed* Facilitate contract signatures by Worldwide Clinical Trials, when applicable* Distribute fully executed Site Agreements or associated documents to sites, eTMF, payment team, Sponsor, and post to internal SharePoint, as applicable* Negotiate Site Agreement amendment language and budgets with sites* Create termination letters or other related documents and send to sites for signature, as applicable* Maintain tracking tools with live, real-time, or regular updates for functional activities* Prioritize effectively and respond to urgent requests within the internal team or from Sponsors* Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.**What you bring to the role**Contract Negotiation:* Proficient in negotiating contract terms with clinical sites and vendors* Ability to identify and address contract issues and disputes efficientlyRegulatory Compliance:* Good understanding of international and local regulatory requirements for clinical trials (e.g., U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), International Council for Harmonization - Good Clinical Practice (ICH-GCP))* Ensure all contracts comply with the latest regulations and guidelinesCommunication:* Excellent verbal and written communication skills for effective interaction with internal stakeholders and clinical sites* Ability to clearly explain contract terms and processes* Strong analytical skills to review and interpret contract terms and financial data* Ability to identify risks and develop mitigation strategiesCollaboration and Teamwork:* Ability to work effectively with cross-functional teams, including legal, finance, and clinical operations* Strong project management skills to handle multiple site contracts simultaneously* Ability to prioritize tasks, manage timelines, and ensure contract deliverables are metTechnical Proficiency:* Proficiency in contract management software and tools* Strong problem-solving skills to address and resolve contract-related issues* Ability to think critically and strategically to overcome challenges* High level of accuracy in reviewing and drafting contracts* Ability to identify and correct discrepancies or potential issues in contract documentation* Understanding of budgeting and financial principles related to clinical trial contracts* Ability to negotiate cost-effective terms and manage financial aspects of contracts* Basic understanding of legal terminology and principles related to contracts* Ability to work closely with legal counsel to ensure all contracts meet legal and regulatory requirements* Strong time management skills to meet deadlines and manage the contract lifecycle efficiently* Ability to handle high volumes of work and work under pressure**Your experience*** Bachelor’s degree or equivalent in business administration, finance, science, or a related field* 1 to 3 years of experience in the Contract Research Organization, pharmaceutical, or clinical research industry, working with investigator/site contracts or a related legal field* Excellent verbal and written English language skills* Proficiency with Microsoft Word, Excel, and Outlook* Knowledge and understanding of International Council for Harmonization (ICH) and Good Clinical Practice (GCP) guidelines, as well as local country legislation and regulatory requirements related to clinical trialsPromotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.