Senior Associate I/II, TMF Operations (LATAM/Remote)
Location: Mexico City, Mexico
Requisition Number: 7038
Position Title: Senior Associate II, TMF Operations
External Description:
Who we are
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works 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 with our customers in improving patients' lives through new and innovative therapies.
Why Worldwide
Everyone plays a vital role in making a 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 Senior Associate I/II does at Worldwide
The Senior Associate II, TMF Operations, is responsible for maintaining Trial Master Files inspection readiness in compliance with the relevant Standard Operating Procedures, ALCOA principles, country regulations, and industry best practices. The Senior Associate II will support the delivery of department objectives in ensuring the management of essential documents. This is a global role and will require working with Worldwide Project Team members and Quality Assurance.
What you will do
- Perform RMC Lead Activities for 3-7 Studies, manage complex studies, or Sponsor portfolio of studies.
- Deputize for RMC Oversight where required.
- Support TMF set-up and coordinate ‘Requests for Sites to be added in eTMF’ between Project Teams (PT) and eTMF administrators, review eTMF access, and coordinate updates as necessary. Provide Subject Matter Expert (SME) support for Project Teams and sponsors related to TMF.
- Oversee the QC process and make sure the RMC is on track (compliant with timelines and documentation) and follow up on non-compliance accordingly.
- Follow-up, raise, and escalate any TMF Quality issues and non-compliances promptly to relevant parties.
- Support Regulatory and Sponsor audits and audits finding resolution, where necessary.
What you will bring to the role
- Excellent written and verbal communication skills to clearly and concisely present information to internal and external parties.
- Ability to exercise sound judgment and ability to identify decisions.
- Proficiency in Microsoft Word and Excel
- Leadership skills
Your experience
- University Degree preferred (Life Science desirable)
- Combination of education plus 2-4 years of relevant experience
- Knowledge of working within a highly regulated industry or understanding 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.
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Employment Type: Regular
Community / Marketing Title: Senior Associate I/II, TMF Operations (LATAM/Remote)
Company Profile:
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.
Location_formattedLocationLong: Mexican Federal District, MX
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