Clinical Data Specialist Position Available at Fortrea in Bangalore

A rare chance for experienced Clinical Data Management professionals has emerged with the Fortrea Clinical Data Specialist role in Bangalore. With a requirement of 3–5 years of experience in Clinical Data Management, this full-time role offers an opportunity to contribute to high-quality clinical trial data management. Interested candidates are encouraged to apply before the deadline.

About Fortrea

Fortrea is a prominent organization operating in the pharmaceutical and life sciences sector, specializing in clinical research and data management. The company is dedicated to ensuring the integrity and quality of clinical trial data, adhering to the highest standards of compliance and regulatory requirements. Fortrea’s commitment to innovation and excellence makes it a significant player in the global clinical research landscape.

Job Title: Clinical Data Specialist

Location: Bangalore, India (Remote)

Experience: 3–5 years in Clinical Data Management

Qualification: Life Sciences, Health Sciences, Information Technology, or Allied Health

Department: Clinical Data Management

Job Type: Full-time

Job ID: 265084

Clinical Data Specialist Job Description

The Clinical Data Specialist will serve as a key member of the project team, primarily responsible for conducting clinical data reviews, generating and resolving queries, and performing reconciliation activities. This role supports the Data Management lead in delivering clinical data that meets client quality and integrity specifications while adhering to project timelines and productivity targets. The specialist will assist in developing the project Data Management Plan and may contribute to setting up data management systems according to project requirements.

Clinical Data Specialist Responsibilities

• Review clinical trial data according to Data Management Plans.
• Perform clinical data review and discrepancy management.
• Generate, track, and resolve clinical data queries.
• Execute reconciliation listings and special data listings.
• Review Edit Check Specifications and Database Specifications.
• Assist in eCRF specification development.
• Support Data Management Plan preparation.
• Perform quality control (QC) of clinical data listings.

Eligibility Criteria

• University/college degree in life sciences, health sciences, information technology, or related subjects.
• Fluent in English, both written and verbal.
• 3 to 5 years of relevant work experience in data management.
• Demonstrated time management skills and ability to adhere to project productivity metrics and timelines.
• Knowledge of medical terminology is preferred.
• Good oral and written communication skills.
• Ability to work in a team environment and collaborate with peers.

Required Skills

• Strong understanding of clinical data management principles.
• Experience with clinical data review, query management, and data cleaning.
• Knowledge of ICH-GCP guidelines.
• Strong analytical and problem-solving skills.
• Ability to manage multiple project timelines.
• Demonstrate good organizational ability and interpersonal skills.
• Constructive problem-solving attitude while meeting deadlines.

How to Apply

Interested candidates can apply for the Clinical Data Specialist position at Fortrea through the official application link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE.

Why Join Fortrea?

Fortrea offers professionals the opportunity to work on global clinical trials with advanced Clinical Data Management processes. Benefits include exposure to international sponsor projects, a hybrid/office work environment, career growth opportunities, and professional development programs.

Note: The application deadline stated in the source notification may have passed. Verify before applying.

Conclusion

The Fortrea Clinical Data Specialist position presents a compelling opportunity for qualified candidates to engage in meaningful work within the clinical data management field. Interested individuals are encouraged to apply at the earliest to secure their chance to contribute to high-quality clinical trial data management.