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 Contracts, does at Worldwide
The Specialist, Site Contracts, is responsible for the development, preparation, negotiation, and finalization, or assistance in the preparation, negotiation, and finalization, of Site Agreements, amendments, and any other documents associated with 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 the returned documents
Review study budgets and costs regarding contract negotiation
Negotiate contract language and budgets with each assigned site through finalization and execution
Escalate site requests outside of preapproved parameters to the Site Contracts Lead for Sponsor review
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 and associated contracts for completeness and accuracy
Finalize contracts and budgets with sites
Perform quality checks of Site Agreements and related documents before the signature process begins
Provide draft or signed contracts and budgets to the regulatory team for submission purposes, when requested
Liaise with the Worldwide Clinical Trials Legal Department, Data Privacy team, study teams, Sponsors, sites, and investigators
Facilitate contract signatures by Worldwide Clinical Trials, when applicable
Distribute fully executed Site Agreements and related documents to sites, electronic Trial Master File (eTMF), payment team, Sponsor, and 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, and regular updates for functional activities
Prioritize effectively and respond to urgent requests within the internal team or from the Sponsor
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:
Regulatory Compliance:
Good understanding of international and local regulatory requirements for clinical trials (e.g., 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 guidelines
Communication:
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 strategies
Collaboration 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 met
Technical 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 pharmaceutical or Contract Research Organization (CRO) 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 ICH-GCP Guidelines, as well as local country legislation and regulatory requirements related to clinical trials
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.
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 .
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law .
