Indirizzo
Forma di lavoro
StipendioWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.
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 you will do
- Serves as a direct Line Manager to Site Contracts Specialists.
- Manages project plans, timelines and resources allocation with regard to activities of the Site Contracts Specialists responsibilities in the designated region.
- Assists in the development and maintenance of departmental processes, policies, SOPs and associated documents.
- Works closely with the Clinical Study Start-up Lead and/or other company departments to ensure delivery of fully executed agreements in support of timely study start-up to meet departmental goals.
- Provides ongoing mentorship and training to Site Contracts Specialists, as needed.
- Assists Global Sites Contracts Management and/or other company departments in leading or participating in department initiatives, tasks forces, and additional training where necessary.
- Negotiation and finalization or assistance in negotiation and finalization of Site Contracts with WCT Legal Department, study team, Sponsors, investigators and/or clinical sites, amending and terminating such contracts
What you will bring to the role
- Extensive knowledge regarding local requirements within the assigned region in regards to clinical trial agreements requirements and negotiations.
- Ability to review and understand technical, medical and legal documents related to clinical trial agreements.
- Excellent leadership skills with ability to work in fast-paced, deadline oriented, and changing environment
- Strong planning, strategizing, managing, monitoring, scheduling, critiquing and problem solving skills
- Excellent written and verbal communication skills, including negotiation skills and knowledge of clinical trial agreements to clearly and concisely present information.
- Computer literacy with document and spreadsheet applications.
Your experience
- At least 5 years of experience as a Site Contract Specialist.
- At least 3 years of previous Line Management experience.
- Bachelor's degree or equivalent in business administration, law, science or related field.
- Adept knowledge of biopharmaceutical/CRO industry and applicable local regulatory requirements.
- Knowledge and understanding of ICH and GCP Guidelines, as well as local regulatory requirements.
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 www.worldwide.com/careers ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .
#LI-MP1 #LI-Remote
