As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.We are looking for full time Associate Manager, Site Agreements who will be responsible of supervision of a team of contract reviewers to ensure the timely and quality delivery of site contract reviews during both study start-up and maintenance .Associate Manager ensures that internal and external expectations are met while identifying and mitigating risks.Associate Manager will be also the line manager for site contract specialists.Job responsibilities: Independently review and negotiate site contracts, confidentiality non-disclosure agreements, and other related documents ("Site Contracts") in accordance with defined processes and timeframes for locations.Develop and maintain database capturing knowledge and understanding of all current client contract processes and assist with the development and facilitation of trainings are in place for the team.Assess and provide solutions regarding the efficacy of the trainings.Maintain up-to-date knowledge of local regulations/laws as applicable, in the context of Site Contracts and provide guidance in the context of Site Contracts.Liaise and communicate with Fortrea corporate Legal and Finance departments, or sometimes refer upwards within Contracts.Provide accurate and concise guidance regarding the financial payment arrangements/processes and legal obligations of the site contracts.Supervise the accurate tracking and progress of site contracts, and assist with maintaining local and public shared electronic files relating to the management of site contracts.Support and assist the local Site Contract Specialist and Clinical Team with legal inputs and directives.With some supervision, assess and develop communication with internal and external customers and contribute to the client partnership development, in particular for new clients.Train and coach less experienced Site contract reviewers and supervise the regional site contract team training and coaching .Assist Site Contract Manager in carrying out other tasks when required, including without limitation, assisting in providing trainings, improving and developing the process, collecting the local offices contract data, template language development and other delegated tasks.May have direct line management responsibility, including without limitation recruitment, training, supervision, utilization and performance review of assigned personnel.Under Site contract manager supervision and guidance, supervise Site contract staff in performance of their day to day work, including if necessary management of resource allocations.Requirements: Work experience in clinical research, including a strong working knowledge of the ICH guidelines and FDA, IRB/IEC regulations University/College degree Flunet local language and English Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.For more information about Fortrea, visit www.fortrea.com.Fortrea is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.We encourage all to apply.For more information about how we collect and store your personal data, please see our Privacy Statement .
