drjobs TMF Specialist II

TMF Specialist II

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Job Location drjobs

Bengaluru - India

Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Job Description

About the job

As a (TMF Specialist II) you will be joining the worlds largest most comprehensive clinical research organisation powered by healthcare intelligence.

Responsibilities:

  • Maintain effective communication with clinical trial teams and CRO staff throughout trial startup maintenance closeout and archive
  • eTMF Health: Manage open Quality Issue (QI) lists for assigned trials to ensure documents which fail TMF quality control and/or TMF quality review are effectively remediated.
  • Closes and reassigns QIs as necessary.
  • eTMF Health: Manage Expected Document Lists (EDL) and counts for the life of assigned trials partnering with the Clinical Trial Team (CTT) and CRO team.
  • Escalate noncompliance with EDL business process to the eTMF Manager as needed.
  • eTMF Health: Provide scheduled and adhoc analysis and metrics on TMF Health for eTMF Managers and CTT/CRO teams on assigned trials.
  • Be responsible for TMF activities for assigned trials including:
  • Supporting TMF document filing into Moderna eTMF system.
  • Maintaining the naming and filing guide specific to TMF documents.
  • Conducting adhoc quality checks and review of document content uploaded into the eTMF.
  • Responding to inquiries regarding TMF management and contents.
  • Supporting inspection/audit preparation and remediation activities.
  • Attend departmental and trialspecific meetings and discussions as required.
  • Maintain up to date knowledge of the TMF Reference Model industry best practices and regulatory requirements.
  • Performs general administrative tasks related to their assigned trials.
  • Completes other TMF documentrelated tasks as required by the eTMF Manager or department head.

Qualifications:

Minimum B.A./B.S. degree preferably in science or healthcare.

2 years work experience preferably in a relevant clinical research setting.

1 years experience in eTMF document management (in a specialized team or as a member of a clinical trial team) is an advantage.

Strong organizational/prioritization skills for the management of workload and attention to detail.

Why ICON

Our focus is to provide you with a comprehensive and competitive total reward package that comprises not only an excellent level of base pay but also a wide range of variable pay and recognition programs. In addition our best in class employee benefits supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career both now and into the future.

Our success depends on the knowledge capabilities and quality of our people. Thats why we are committed to developing our employees in a continuous learning culture one where we challenge you with engaging work and where every experience adds to your professional development.

ICON including subsidiaries is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race colour religion sex sexual orientation gender identity national origin disability or protected veteran status.

If because of a medical condition or disability you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of a position please let us know.

Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

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Remote Work :

No

Employment Type

Full Time

About Company

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