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Engaged Employer

Fortrea Development India Private Limited

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3.9

based on 687 Reviews

24 Fortrea Development India Private Limited Jobs

Associate Validator II

Fortrea

3.9

based on 687 Reviews

1-3 years

Bangalore / Bengaluru

1 vacancy

Associate Validator II

Fortrea Development India Private Limited

posted 12d ago

Job Role Insights

Flexible timing

Key skills for the job

Pharmacovigilance Stock Market Dentistry Clinical Research Bioinformatics Clinical Data Management

+ 10 more

Job Description

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Job Overview:

Serve as a member of the project team with primary responsibility for all documentation requirements in support of Global EDC Solutions tasks to include receiving and logging-in and scanning contractual and validation documentation. Assist project teams with validation tasks as requested, i.e., with the creation, production, printing and tracking of study documentation and controlled documents.

Summary of Responsibilities:

Serves as a member of the project team with primary responsibilities for all documentation, requirements to support global EDC solutions tasks.
Assist project teams with validation tasks as requested.
Assist with creation, production, printing and tracking of study documents and other controlled documents as needed.
Create and Execute validation test scripts as requested and document the test results.
Ensure quality of work.
Prioritize workload to meet specified completion dates.
Assist with the maintenance of validation metrics.
Carry out all activities according to Fortrea Standard Operation Procedures (SOPs) and project specific conventions within the framework of Quality Management and Good Clinical Practice (GCP)/ICH guidelines.
Maintain accurate records of all work performed.
Perform other duties as assigned by management.
Assist with special projects as designated.
And all other duties as needed or assigned.