Trial Master File (TMF) Senior Support Analyst

TransPerfect Inc

Pune District

On-site

INR 900,000 - 1,500,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

TransPerfect Life Sciences is seeking a Trial Master File Senior Support Analyst (TMF SSA) in Pune district, India. The role ensures accuracy of clinical documentation within the TMF and mentors TMF Associate Support Analysts.

You will oversee TMF quality reviews, support audits/inspections, and generate TMF metrics while aligning with SOPs and regulatory requirements.

Qualifications

  • Bachelor’s degree in Clinical Research, Life Sciences or Business.
  • Minimum 4 years’ TMF experience or equivalent.

Responsibilities

  • Perform document level Quality Checks.
  • Index and/or activate documents in an eTMF.
  • Migrate Paper/Electronic TMFs.
  • Provide Audit/Inspection support.
  • Perform TMF Quality Reviews.
  • Remediate findings from TMF Quality Reviews.
  • Generate reports and metrics.
  • Author and maintain TMF Management Plans and tools.
  • Create milestones, events and placeholders in the eTMF.
  • Create and maintain storyboard(s).
  • Meet with study teams to understand events impacting TMF.
  • Oversee TMF Support Analysts and conduct quality spot checks.
  • Serve as a TMF Subject Matter Expert (SME).
  • Escalate issues to LMK TMF Project Manager as appropriate.
  • Maintain documentation evidencing above activities.

Skills

Problem solving
Analytical thinking
Communication skills
English proficiency
Under pressure
Global collaboration
eTMF knowledge

Education

Bachelor’s degree in Clinical Research/Life Sciences/Business

Tools

Microsoft Office

Job description

OVERVIEW:

The Trial Master File Senior Support Analyst (TMF SSA) is the Quality Control Expert and ensures accuracy and completeness of all clinical documentation within the TMF and is expected to perform these responsibilities independently. This role is also tasked with mentoring TMF Associate Support Analysts (TMF ASA). The clinical trial documentation must be consistent with the Trial Master File Specifications, submission/inspection readiness criteria and comply with LMKs (or clients) SOPs and regulatory requirements and provides updates to leadership, as relevant.

DESCRIPTION:
  • Perform document level Quality Checks

  • Index and/or activate documents in an eTMF.

  • Migrate Paper/Electronic TMFs

  • Provide Audit/Inspection support

  • Perform TMF Quality Reviews

  • Remediate findings resulting from TMF Quality Reviews

  • Generate reports and metrics

  • Author and maintain TMF Management Plans and management tools

  • Create and maintain milestones, events and placeholders or equivalent in the eTMF

  • Create and maintain storyboard(s)

  • Meet with study team(s) to understand events/activities that would impact the TMF

  • Support LMK TMF Project Manager with performing TMF Support Analyst oversight and quality spot checks

  • Serve as a TMF Subject Matter Expert (SME)

  • Escalate issues to LMK TMF Project Manager(s), as appropriate

  • Maintain any and all documentation to evidence the above

  • Complete all other tasks that are deemed appropriate for this role and assigned by the manager/supervisor.


REQUIRED SKILLS:
  • Strong problem-solving and analytical skills, with the ability to think strategically and act tactically

  • Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint, and Teams)

  • Excellent customer service skills with the ability to balance multiple tasks

  • Superior written and spoken communication skills in English

  • Ability to work under pressure and meet deadlines

  • Ability to work in a global environment with internal and external partners

  • Knowledge of eTMF platforms and interoperability with clinical research systems

  • Aptitude for forging strong partnerships/relationships across the organization including operations, business development, production, and quality and customers.

REQUIRED EXPERIENCE & QUALIFICATION:
  • Minimum Bachelor’s degree to its equivalent in Clinical Research, Life Sciences or Business

  • Minimum 4 years’ experience in Trial Master File (TMF) or professional equivalent.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Trial Master File (TMF) Senior Support Analyst
Trial Master File (TMF) Senior Support Analyst

TransPerfect • Pune District, Pimpri-Chinchwad

On-site
INR 1,200,000 - 1,800,000
TMF Lead I
TMF Lead I

F5 Remote Jobs • India

Remote
INR 1,200,000 - 1,800,000
TMF Lead
TMF Lead

Tilda Research Inc. • India

On-site
INR 1,600,000 - 2,600,000
Sr. Manager, TMF Process Lead
Sr. Manager, TMF Process Lead

Bristol Myers Squibb • Hyderabad

On-site
INR 2,000,000 - 4,000,000
Configuration Specialist I
Configuration Specialist I

Transperfect • Pune District

On-site
INR 450,000 - 700,000
FSP Clinical Trial Coordinator - eTMF
FSP Clinical Trial Coordinator - eTMF

ThermoFisher Scientific • Mumbai

On-site
INR 600,000 - 1,000,000
Sr. Manager, TMF System Business Lead
Sr. Manager, TMF System Business Lead

Bristol Myers Squibb • Hyderabad

On-site
INR 3,500,000 - 6,500,000
Sr. Manager, TMF Process Lead
Sr. Manager, TMF Process Lead

0617 Bristol-Myers Squibb Business Services India Private Limited • Hyderabad

Hybrid
INR 1,200,000 - 1,800,000
Flexible work models
Remote-by-design options
Associate Director, TMF Operations
Associate Director, TMF Operations

Syneos Health, Inc. • Hyderabad

On-site
INR 3,500,000 - 6,000,000
FSP Clinical Trial Coordinator - eTMF
FSP Clinical Trial Coordinator - eTMF

Jobgether • India

On-site
INR 800,000 - 1,100,000