
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
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10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
âą Lead end-to-end site contracting for clinical trials, ensuring timely and effective contract execution âą Monitor and report on critical metrics including cycle times, contract quality, and compliance throughout the contract lifecycle âą Develop and implement contracting strategy documents, templates, and best practices that drive efficiency and consistency âą Collaborate with global teams on investigator grant budgets and fee parameters âą Manage project-specific contracting teams, providing leadership, training, and mentorship âą Identify and mitigate risks related to timelines, budgets, strategy effectiveness, and quality âą Maintain transparent communication with sponsors, internal teams, vendors, CROs, and sites âą Build and strengthen relationships across internal and external partners to expedite contract execution âą Support Clinical Operations, Feasibility, Business Development, and Investigator Payments âą Provide regular performance updates and insights to clients and senior management âą Ensure accurate budget tracking and resource forecasting for the contracting team
âą 3 to 8 years of experience (depending on level) within a CRO or related field âą Bachelor's degree in law, business, economics, or related field (or equivalent industry experience) âą Strong negotiation and contract management skills with ability to interpret complex legal language âą Excellent leadership, diplomacy, and interpersonal skills with proven ability to influence across teams âą Outstanding organizational and project management abilitiesâcomfortable juggling multiple concurrent projects âą Advanced proficiency in Excel, Word, and PowerPoint âą Strong analytical skills and attention to detail âą Experience with contract management systems and eTMF platforms âą Ability to thrive in virtual, multicultural, and cross-timezone environments âą Demonstrated thought leadership, problem-solving ability, and grace under pressure âą Must be living in Serbia, Poland, Ukraine, Romania, or Hungary and have the right to work in the applicable country
âą Ownership of a critical function that directly impacts trial success âą Exposure to diverse therapeutic areas and global operations âą Work with talented cross-functional teams
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