Associate II, TMF Operations - UK - Remote

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 prioritise 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 Records Management Compliance Department does at Worldwide
TMF Operations handles the processing, maintenance and archiving of all essential documents in strict accordance with pertinent Standard Operating Procedures, country-specific regulations, and industry best practices. Throughout Worldwide Clinical Trials, our culture of collaboration and innovation is what propels us in our pursuit of excellence in clinical research and making a meaningful impact on every patient's life. Roles within our TMF Operations department have a global scope, with the opportunity to regularly collaborate with members of the Worldwide Project Team.

What you will do

• Fulfil the "TMF Approver" and/or "TMF QC Reviewer" roles as defined by the relevant Standard Operation Procedure(s) (SOP) and working practices.
• Process, review, and resolve rejected Trial Master File (TMF) documents, for complex studies or Sponsor portfolio of studies both in an electronic and hard copy format.
• Prepare periodic TMF Quality Control checklists for review by Project Team review.
• Perform periodic TMF Quality Control to ensure adherence to regulatory, ICH GCP, Sponsor, and industry best practices.
• Work with a variety of Electronic Document Management and electronic TMF Systems to review, classify and process Essential Documents.

What you will bring to the role

• Possess data collection, indexing and editing skills, including ability to adhere to standardised document naming conventions.
• Possess excellent written and verbal communication skills to clearly and concisely present information.
• Display strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment.
• Handle multiple, highly detailed tasks with exceptional accuracy. Demonstrate strong planning and organisational skills.
• Demonstrate proficiency in Microsoft Word and Excel.
• Develop proficiency in use of an electronic document repository or eTMF. General understanding of clinical research principles and processes.

Your experience

• Minimum 6 months of administrative experience, preferably but not strictly in the CRO or Pharma industry.
• Knowledge of working within a highly regulated industry (desirable).
• A strong, long-term interest in administrative-focused work, with close attention to detail and comfort handling routine, process-driven tasks.

We love knowing that someone is going to have a better life because of the work we do.