
FSP Site Contract Specialist
Posted Sep 8

Posted Sep 8
This is a fully remote position, open to applicants in Brazil.
• Prepare, evaluate, negotiate, and finalize agreements with study sites in accordance with local and accepted protocols.
• Negotiate investigator grant budgets, along with contractual terms and conditions, while adhering to approved guidelines.
• Ensure adherence to negotiation parameters, authority approvals, contractual processes, client expectations, budget guidelines, templates, and established procedures.
• Identify and evaluate legal, financial, and operational risks, escalating issues as necessary.
• Offer recommendations and alternative solutions for investigator contract negotiations.
• Collaborate with internal functional departments to synchronize site startup and contractual activities with agreed-upon timelines.
• Align contract negotiation efforts with the critical path for site activation.
• Meet target cycle times for site activations.
• Escalate any out-of-parameter issues through the established communication channels.
• A Bachelor's degree or an equivalent and relevant formal academic/vocational qualification.
• 2–5 years of prior experience that provides the knowledge, skills, and abilities necessary for this role.
• A combination of relevant education, training, and/or directly related experience may be deemed sufficient.
• Strong understanding of contract law, including aspects of business, intellectual property, local tax, and stamp laws.
• Capability to apply fundamental principles of investigator grant negotiation.
• General knowledge of business and financial principles related to service agreements.
• Proficient verbal and written communication skills in both English and the local language.
• Ability to draft and negotiate contract provisions and budgetary matters within defined parameters, with suitable oversight.
• Keen attention to detail.
• Exceptional analytical and decision-making skills.
• Familiarity with pharmaceutical product development and the role of CROs.
• Capacity to work independently as well as collaboratively within a team.
• Strong organizational and time management skills.
• Working knowledge of PPD SOPs and WPDs.
• Ability to prioritize competing tasks and assess contractual risks and issues.
• Proficient in using automated systems and computerized applications.
• Customer-oriented communication, problem-solving, and collaboration abilities.
• Capability to remain upright and/or stationary for 6–8 hours a day.
• Ability to perform repetitive hand movements.
• Frequent mobility is required.
• Ability to lift and carry weights of 15–20 lbs.
• Regular and consistent attendance is a must.
• Fully remote work arrangement.
• Standard Monday-Friday work schedule.
IQVIA
CTI Clinical Trial and Consulting Services
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