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Trial Master File Associate
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Trial Master File As....
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Trial Master File Associate

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1 Vacancy
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Job Location

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Warszawa - Poland

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2784401

TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full servicecapabilities resourcing and Functional Service (FSP) solutions.

Join Our Team as a Trial Master File Associate (TMF Associate) home based in Poland.

About this role

TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full servicecapabilities resourcing and Functional Service (FSP) solutions.

As part of our Clinical Operations Unit team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals.

The Trial Master File Associate (TMF Associate) is part of the Clinical Operations Unit within TFS Clinical Development Services (CDS) and will function operationally as a member of the Study Team with the responsibility to create organize maintain and oversee the Trial Master File (TMF) according to company policies SOPs Work Instructions and regulatory requirements.

Key Responsibilities

Create the Study TMF Index as directed by the PM (Project Manager)

Create first draft of TMF Plan implement changes after review generate final version and distribute final version to the study team

Create TMF at Trial Country and Site Level (paper TMF)

Request IT to create eTMF at Trial Country and Site Level when TFS system is used

Inform to study team that TMF is created and ready for document submission

Actively follow up study team is submitting documentation following the process described in The TMF Plan

Actively collaborates in the training to study Team in regards to the TMF workflow and management

Qualifications:

Bachelors Degree preferred Knowledge of GCP/ICH guidelines

Good English written and communication skills

Good organizational and multitasking skills

Good software and computer skills

Able to work in a fast paced environment with changing priorities

Able to effectively work in a team environment

Effective time management

    What We Offer

    We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll be joining a team that values collaboration innovation and making a difference in the lives of patients

    A Bit More About Us

    Our journey began over 25 years ago in Sweden in the city of Lund. As a global CRO with the ultimate goal of ensuring patients safety and wellbeing we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe North America Asia Pacific and the Middle East.

    Our core values of Trust Quality Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization.

    #Together we make a difference

    Employment Type

    Full Time

    Company Industry

    About Company

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