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 3,500+ 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
Perform RMC Lead Activities for 3-7 Studies, manage complex studies or Sponsor portfolio of studies
Support TMF set-up, coordinate ‘Requests for Sites to be added in eTMF’ between Project. Teams (PT) and eTMF administrators; review eTMF access and coordinate updates as necessary
Communicate directly with multiple Project Team members and Sponsors to assess project needs relevant to the TMF.
Provide Subject Matter Expert (SME) support for Project Teams and Sponsor related to TMF.
Oversee the QC process and makes sure the RMC is on track (compliant with timelines and documentation) and follow up on non-compliance accordingly.
Prepare, maintain, and share TMF metrics and spreadsheets for assigned studies with Project Teams and Sponsors. Review TMF Key Performance Indicators (KPIs) and makes sure that TMF KPIs are in compliance.
What You Will Bring To The Role
Possess excellent written and verbal communication skills to clearly and concisely present information to internal and external parties
Work independently and with teams (internal and external) and handle multiple, highly detailed tasks with exceptional accuracy
Ability to work under pressure
Display strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment
Your Experience
University Degreed preferred (Life Science desirable)
Combination of education plus 2-4 years of relevant experience
Knowledge of working within a highly regulated industry or experience of CRO/Pharmaceutical Company industry
Why Worldwide
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.
We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.
Seniority level
Not Applicable
Employment type
Full-time
Job function
Research, Science, and Administrative
Industries
Biotechnology Research and Pharmaceutical Manufacturing
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