eTMF Specialist

Posted 13 Days Ago
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Cambridge, MA
Mid level
Biotech
The Role
The TMF Specialist oversees documentation processes in clinical studies, ensuring compliance with regulatory standards and engaging cross-functional teams and vendors.
Summary Generated by Built In

The Opportunity:

As the TMF Specialist, you will be responsible for working across clinical study teams in line with TMF processes across the development portfolio, with regards to the filing and maintenance activities for clinical studies during the study start-up, maintenance and close-out periods. To be successful, you will be detail-oriented, with a flexible and solution-oriented outlook and the ability to support team members within Relay Therapeutics and with our CRO partners under the guidance of the Sr. Manager, eTMF.

 Your Role:

  • You will engage in assessing eTMF metrics for completeness, timeliness, and quality.
  • You will facilitate TMF QC Reviews and ensure issues identified are tracked to resolution. 
  • You will help build and maintain strong partnership with key stakeholders to ensure cross-functional eTMF engagement.
  • You will engage with CROs/Vendors to ensure responsibilities around eTMF are clearly defined and executed.
  • You will contribute to eTMF study creation, maintenance, and archival, ensuring all activities are performed in accordance with Relay’s Standard Operating Procedures (SOPs), ICH-GCP Guidelines, EMA, FDA, and other health authority requirements.
  • You will help identify business needs to assess the current state of eTMF and identify opportunities for process improvement, ensuring industry best practice is implemented.
  • You will participate in the creation and review of Study-specific eTMF Plans, Study-specific TMF Indexes, and QC approach across all studies.
  • You will participate in discussions with IT and eTMF system managed services relations and topics.
  • You may participate in health authority inspections and audits.

  Your Background:

  • You have 2-5 years industry experience with TMF/eTMF.
  • You have hands-on experience with TMF QC processes, including both individual document quality checks and TMF completeness reviews.
  • You have working knowledge of ICH-GCP, FDA, and EMA regulations.
  • You have working knowledge of the CDISC TMF Reference Model.
  • Veeva Vault eTMF experience a plus.
  • You are a motivated self-starter who has demonstrated critical thinking skills.
  • You have excellent organizational skills with the ability to multi-task and prioritize effectively in an extremely fast-paced and dynamic environment.
  • You have outstanding verbal and written communication skills, allowing for an open and effective dialogue throughout the organization.
  • You have a strong work ethic, excellent problem-solving ability, and attention to detail and quality are critical to success.

#JO1

About Relay Therapeutics

Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.  

Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you’re excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us! 



Top Skills

Cdisc Tmf Reference Model
Ema
Fda
Ich-Gcp
Veeva Vault Etmf
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The Company
HQ: Cambridge, MA
344 Employees
On-site Workplace
Year Founded: 2016

What We Do

Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, our approach combines unprecedented computational power with leading-edge experimental approaches across the fields of structural biology, biophysics, chemistry and biology. By applying these insights, we believe we have a differentiated approach to drug protein targets based on their motion, enabling us to select and advance unique product candidates that can be developed into novel therapies for patients.

Located in Cambridge, Massachusetts, our world-class team is equal parts bright and bold, with a shared passion for working in intellectually stimulating environments. If you're creative, collaborative and passionate about making a difference in the lives of patients, join us!

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