Senior TMF Specialist - Hayward

Only for registered members Hayward, United States

2 weeks ago

Default job background
$118,000 - $131,000 (USD)

Job summary

This position is responsible for collecting, reviewing, maintaining and archiving essential regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP) guidelines.

Responsibilities including but not limited to:
  • Work directly with TMF Content Owners to identify issues perform completeness checks and upload documents to the eTMF
  • Acting as TMF subject matter expert SME/point of contact for study teams and TMF stakeholders.

Lorem ipsum dolor sit amet
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.

Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.

Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Get full access

Access all high-level positions and get the job of your dreams.



Similar jobs

  • Work in company Remote job

    Senior TMF Specialist

    Only for registered members

    This position is responsible for collecting reviewing maintaining and archiving essential regulatory documents for the Trial Master File TMF in accordance with Good Clinical Practice GCP E6 ICH Guidelines and other regulatory guidance documents relevant regulations e.g. 21 CFR Pa ...

    Hayward, CA

    2 weeks ago

  • Work in company

    Senior TMF Specialist

    Only for registered members

    This position is responsible for collecting and maintaining essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents. · ...

    Hayward $118,000 - $131,000 (USD) Full time

    2 weeks ago

  • Work in company

    Sr. TMF Specialist

    Only for registered members

    This position is responsible for collecting, reviewing, maintaining and archiving essential regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents. The Senior Clinical Documen ...

    Brisbane Freelance

    1 month ago

  • Work in company

    Sr. TMF Specialist

    Only for registered members

    +This position is responsible for collecting and maintaining essential Regulatory documents for the Trial Master File (TMF) · +• Work directly with TMF Content Owners to identify issues · • Review and classify documents collected from internal and external sources · • Reconcile e ...

    Brisbane Freelance

    1 month ago

  • Work in company Remote job

    Sr. TMF Specialist

    Only for registered members

    This position is responsible for collecting, reviewing, maintaining, · and archiving essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, · relevant regulations ( ...

    Brisbane, CA Freelance

    1 month ago

  • Work in company

    Clinical Records Specialist I

    Only for registered members

    A Clinical Records Specialist I assists in the quality review and processing of trial related records based on applicable regulations. · ...

    Newark $74,000 - $90,000 (USD)

    1 month ago

  • Work in company

    Clinical Records Specialist I

    Only for registered members

    A Clinical Records Specialist with excellent attention to detail and communication/organizational skills is needed to assist in quality review, tracking and processing of trial related records based on GCP/ICH regulations. · Conduct quality reviews on trial records according to a ...

    Newark $74,000 - $90,000 (USD) Full time

    1 month ago

  • Work in company

    Clinical Records Specialist I

    Only for registered members

    A Clinical Records Specialist I will assist in the quality review, tracking and processing of trial related records based on applicable Good Clinical Practice (GCP)/International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) regulatio ...

    Newark $74,000 - $90,000 (USD)

    1 month ago

  • Work in company

    Clinical Records Specialist I

    Only for registered members

    Ardelyx is seeking a Clinical Records Specialist I with excellent attention to detail and communication/organizational skills. · Conduct quality reviews on trial records. · Apply proper classification and metadata to essential records. · ...

    Newark, CA

    1 month ago

  • Work in company

    Clinical Records Specialist I

    Only for registered members

    A Clinical Records Specialist I assists in quality review, tracking, and processing of trial related records based on applicable Good Clinical Practice (GCP) regulations. · Conduct quality reviews on trial records according to GCP/ICH regulations · ...

    Newark, CA

    1 month ago

  • Work in company

    Clinical Records Specialist I

    Only for registered members

    A Clinical Records Specialist I will assist in the quality review and processing of trial related records based on GCP/ICH regulations and company SOPs. · ...

    Newark, CA

    2 weeks ago

  • Work in company

    Trial Master File Specialist

    Only for registered members

    Seeking a talented experienced contract Trial Master File Specialist with a passion for new cancer therapy development. · ...

    South San Francisco

    1 week ago

  • Work in company

    Senior Clinical Trials Specialist

    Only for registered members

    The Senior Clinical Trials Specialist coordinates clinical trials activities. · Review study documents · ...

    Alameda, CA

    6 days ago

  • Work in company

    Trial Master File Specialist

    Only for registered members

    Seeking a talented, · experienced contract Trial Master File · Specialist with a passion for new cancer therapy development. · ...

    South San Francisco, CA

    1 week ago

  • Work in company

    Senior Clinical Trials Specialist

    Only for registered members

    The Senior Clinical Trials Specialist coordinates the activities associated with the evaluation, initiation, and management of clinical trials. This role provides operational support to the Study Delivery Lead (SDL) by managing assigned study activities and clinical sites, · Revi ...

    Alameda $114,500 - $163,500 (USD)

    1 week ago

  • Work in company

    Senior Clinical Trials Specialist

    Only for registered members

    The Senior Clinical Trials Specialist coordinates the activities associated with the evaluation, initiation, and management of oncology clinical trials.Provides operational support to the Study Delivery Lead (SDL) by managing assigned study activities and clinical sites. · ...

    Alameda $108,500 - $153,000 (USD)

    1 month ago

  • Work in company

    Senior Clinical Trials Specialist

    Only for registered members

    The Senior Clinical Trials Specialist coordinates clinical trials activities by managing assigned study activities and clinical sites. · Review study documents to manage clinical trials, · Provide CRO oversight on activities related to site start-up and maintenance, · Participate ...

    Alameda $114,500 - $163,500 (USD) Full time

    1 week ago

  • Work in company

    Clinical Trial Associate

    Only for registered members

    The Clinical Trial Associate is developing project plans and providing reports to inform decision making by the Project Leader and Functional Leads. · Minimum 2 years' experience in Clinical Research organization or pharma organization. · Good understanding of how their role inte ...

    San Francisco

    3 weeks ago

  • Work in company

    Clinical Trial Associate

    Only for registered members

    +The Clinical Trial Associate is developing project plans and providing reports to inform project oversight and decision making+ · +The CTA will be assigned to Biotech and Enterprise projects+ ...

    San Francisco, CA

    2 weeks ago

  • Work in company

    Clinical Trial Manager

    Only for registered members

    +This is an opportunity for an experienced Clinical Operations Professional to manage clinical trials in an industry setting. · +Clinical operations functional activities related to the execution of assigned clinical trials based upon department and corporate goals and objectives ...

    San Francisco $120,000 - $150,000 (USD)

    1 month ago