Senior Specialist

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 Sr. Specialist, Site Contracts Does At Worldwide Senior Specialist, Site Contracts is responsible for developing, reviewing, and assisting with the negotiation of Site Agreements with Institutions and Investigators and providing oversight and expertise to all site contract activities during all stages of a Clinical Trial. This includes the development of investigator grants, Clinical Trial Agreement templates and applicable plans, negotiation of Clinical Trial Agreements and ancillary agreements, and mitigation of site contracting risks. What You Will Do Prepare country contract templatesDraft and send Site Agreements or any contracts associated with sites to begin negotiationsProvide site contract execution planned timelines and site negotiation statusSend items for translation, if applicable, and receive and translate itemsReview study budgets and costs pertaining to contract negotiationNegotiate contract language and budgets with each assigned site through finalization and executionEscalate sponsor site requests outside of preapproved parametersEscalate risks and non-responsive sites to the Site Contracts Lead or internal team, as applicableIf required to provide equipment to sites, ensure appropriate information or appendices are added to Site Agreements or associated documentsCreate donation agreements, as applicableReview Site Agreements or any associated contracts for completeness and accuracyFinalize contracts and budgets with sitesPerform quality checks of Site Agreements or associated contracts before the signature process beginsIf requested, provide draft or signed contracts and budgets to the regulatory team for submission purposes, where neededLiaise with Worldwide Clinical Trials Legal Department, Data Privacy team, study teams, sponsors, sites, investigators, and other stakeholdersFacilitate contract signatures by Worldwide Clinical Trials, when applicableSend fully executed Site Agreements or associated documents to sites, electronic Trial Master File (eTMF), payment team, sponsors, and post to internal SharePoint, as applicableNegotiate Site Agreement amendment language and budgets with sitesCreate termination letters and send them to sites for signature, as applicableMaintain tracking tools with live, real-time updates for functional activitiesPrioritize effectively and respond to urgent requests within the internal team or sponsorReview Trial Master File (TMF) structure, oversee Investigator Grants Budgets, and ensure quality checks for site agreementsAct as a lead and subject matter expert on site agreements and related processes, prepare and update contract templates, coordinate master budgets and contract and budget plans, send these to the sponsor, and manage site agreementsMaintain tracking tools, communicate site contracting strategies, timelines, and tracking requirements, and escalate issues as necessaryDevelop mitigation plans, resolve contract negotiation issues, and contribute to process improvement initiativesPerform 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 Advanced Contract NegotiationProficient in negotiating complex contract terms with clinical sites and vendorsSkilled in resolving contract issues and disputes efficientlyRegulatory ComplianceThorough 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 Harmonisation - Good Clinical Practice [ICH-GCP])Ensures all contracts comply with the latest regulations and guidelinesCommunicationExcellent verbal and written communication skills for effective interaction with internal stakeholders and clinical sitesAbility to clearly explain complex contract terms and processesStrong problem-solving skills to address and resolve contract-related issuesAbility to think critically and strategically to overcome challengesCollaboration and TeamworkAbility to work effectively with cross-functional teams, including legal, finance, and clinical operationsSkilled in fostering a collaborative work environmentTechnical ProficiencyProficiency in contract management software and toolsHigh level of accuracy in reviewing and drafting contractsAbility to identify and correct discrepancies or potential issues in contract documentationUnderstanding of budgeting and financial principles related to clinical trial contractsAbility to negotiate cost-effective terms and manage financial aspects of contractsBasic understanding of legal terminology and principles related to contractsAbility to work closely with legal counsel to ensure all contracts meet legal and regulatory requirementsStrong time management skills to meet deadlines and manage the contract lifecycle efficientlyAbility to handle high volumes of work and perform under pressureStrong project management skills to oversee multiple site contracts simultaneouslyAbility to prioritize tasks, manage timelines, and ensure contract deliverables are metAdvanced analytical skills to review and interpret contract terms and financial dataAbility to identify risks and develop mitigation strategies Your Experience 3 to 5 years of experience as a Contract Specialist in the clinical research, pharmaceutical, or Contract Research Organization industryBachelor's degree or equivalent in Business Administration, Finance, Science, or a related fieldExcellent verbal and written English language skillsProficiency with Microsoft Word, Excel, and OutlookKnowledge and understanding of International Council for Harmonisation (ICH) and Good Clinical Practice (GCP) Guidelines, as well as local country legislation in the sphere of clinical trials and local regulatory requirements Promotion 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. At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation. The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates): United States of America - $71,500.00 - $142,500.00 The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.