Associate II, TMF Operations - Mexico/Argentina/Brazil - Remote

Worldwide Clinical Research S. de R.L. de C.V.; México; A distancia; USD 40,000 - 60,000; Jornada completa

Descripción de la vacante

Join a global CRO as an Associate II, TMF Operations, responsible for managing essential documents and overseeing quality control in clinical trials. This remote role requires a strong background in document management and interpersonal skills to thrive in a fast-paced environment.

Formación

• 1-2 years of relevant experience required.
• Knowledge of working within a highly regulated industry is desirable.
• Proficiency in using electronic document repositories.

Responsabilidades

• Process and review TMF documents for complex studies.
• Perform TMF Quality Control to ensure regulatory adherence.
• Communicate issues and trends to RMC Lead.

Conocimientos

Interpersonal skills

Document recognition

Proficiency in Microsoft Word

Proficiency in Microsoft Excel

Educación

University Degree (Life Science preferred)

Descripción del empleo

Associate II, TMF Operations - Mexico/Argentina/Brazil - Remote page is loaded

Associate II, TMF Operations - Mexico/Argentina/Brazil - Remote

Apply remote type Remote locations Mexico City, Mexico time type Full time posted on Posted 9 Days Ago job requisition id JR100955

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 Associate II, TMF Operations does at Worldwide

The Associate II, TMF Operations is responsible for the processing, maintaining and archiving of all essential documents in compliance with the relevant Standard Operating Procedures, ALCOA principles, country regulations and industry best practice. The Associate will support the delivery of department objectives in ensuring the management essential documents. This is a global role and will require working with Worldwide Project Team members.

What you will do

• 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.
• 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.
• Communicate directly with RMC Lead to report trends and issues relevant to the TMF.
• Escalate any TMF Quality issues in a timely manner to RMC Lead.
• Provide administrative support for the RMC Lead including but not limited to filing and maintaining internal documents on study SharePoint (TMF Quality Control checklists and different trackers).

What you will bring to the role

• Proficiency in use of an electronic document repository or eTMF, and document recognition skills.
• Strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment
• Sound judgment and ability to identify decisions requiring supervisory approval.
• Proficiency in Microsoft Word and Excel.

Your experience

• University Degree preferred (Life Science desirable)
• 1-2 years of relevant experience
• Knowledge of working within a highly regulated industry (desirable)

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’reon a mission to hire thevery bestand 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.