Associate I, Tmf Operations

hace 2 semanas

Ciudad de México Worldwide Clinical Trials A tiempo completo

**Requisition Number**
**6707**

**Employment Type***:
**Regular**

**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 almost 2,500 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.

**What you will do**
- Fulfil the "TMF Approver" and/or "TMF QC Reviewer" roles as defined by the relevant Standard Operation Procedure(s) (SOP)
- Process Trial Master File (TMF) documents for multiple 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
- Communicate directly with Project Team members to assess project needs relevant to the TMF
- Escalate any TMF Quality issues in a timelines manner to relevant parties
- Prepare and transmit TMF and other critical documents to the Sponsor in accordance with the relevant instructions
- Perform additional tasks as assigned by their Line Manager

**What you will bring to the role**
- Possess data collection, indexing and editing skills, including ability to adhere to standardized document naming conventions
- Possess excellent written and verbal communication skills to clearly and concisely present information
- Work independently and with teams and can execute tasks works under general direction, seeks assistance as needed
- Display strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment
- Exercise sound judgment and ability to identify decisions requiring supervisory approval
- Handle multiple, highly detailed tasks with exceptional accuracy
- Demonstrate strong planning and organizational skills
- Demonstrate proficiency in Microsoft Word and Excel
- Develop proficiency in use of an electronic document repository or eTMF
- Understand and adhere to corresponding Worldwide and sponsor standard operating procedures
- General understanding of clinical research principles and processes

**Your experience**
- University Degree preferred ( Life Science desirable )
- Up to 1 year of relevant experience
- Knowledge of working within a highly regulated industry (desirable)

**Why Worldwide**

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

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