Associate Validator II
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 12h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 22d ago
The date the source published, not the day we noticed it (2026-09-10). Last seen at its source 1h ago.
We have tracked this listing since 22 Sep 2026 (9 days). The employer's own board has carried it every time we have read it, most recently 1 hour ago.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
India
The description states no restriction of its own. This is the source's own tag.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
workday employer's own board first seen 9d ago · last seen 1h ago
- location not stated
The listing
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.
Qualifications (Minimum Required):
- University / college degree (life sciences, health sciences, information technology or related subjects) or a certification in allied health professions from an appropriate accredited institution.
- Fluent in English, both written and verbal.
Experience (Minimum Required):
- 2–4 years of experience in CDM and EDC testing, with hands-on expertise in Rave and Veeva.
- A neat, methodical, and thorough approach to the work with an emphasis on attention to detail.
- Good concentration skills are required to meet the consistently high standards expected.
- Self-motivation with the ability to work under pressure to meet demanding deadlines.
- Effective communication skills and the ability to work as part of a team.
Preferred Qualifications Include:
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Physical Demands/Work Environment:
- Remote-Based, as requested by the line manager
- Work Timings: Should be flexible to accommodate shift-based working hours.
Learn more about our EEO & Accommodations request here.