Are you looking for a career opportunity in Clinical Data Management, data validation, or clinical research? JSS Medical Research has announced an exciting opportunity for the position of Validation Associate in Faridabad.

The Validation Associate role involves supporting clinical studies through data validation, query management, database testing, CRF review, external data validation, SAE reconciliation, and clinical data quality activities.

Candidates with backgrounds in BDS, BAMS, BHMS, Life Sciences, Pharmaceuticals, and Clinical Research may be eligible based on the requirements mentioned in the job description.

This is a valuable opportunity for candidates interested in building a career in Clinical Data Management (CDM) and clinical trial data operations.

Job Details

Validation Associate Job Responsibilities

As a Validation Associate, the selected candidate will support clinical data validation and database-related activities for clinical studies.

Key responsibilities include:

• Preparing and updating the Annotation List according to study requirements.
• Assisting with the preparation of the Data Validation Plan.
• Developing and updating Edit Check Specifications.
• Supporting the preparation of database and data entry screens.
• Preparing the Operational Manual for EDC trials.
• Developing CRF Filling Guidelines for clinical studies.
• Performing query management activities according to study requirements.
• Raising and resolving manual queries generated by the data entry team and medical coders.
• Conducting quality checks for form updates and reverification activities.
• Supporting CRF data entry and database testing.
• Validating external data after it is uploaded into the clinical database.
• Performing SAE and laboratory data reconciliation.
• Updating Self-Evident Correction queries and related documentation.
• Maintaining reports and study trackers on a regular basis.
• Completing additional activities assigned by the supervisor or department.

Required Knowledge and Skills

Candidates applying for this Validation Associate job should have knowledge of clinical research and clinical data processes.

Required Knowledge

Candidates should have knowledge of:

• MS Office
• Basic Clinical Research
• Clinical Trials
• Good Clinical Practices (GCP)
• Good Documentation Practices (GDP)
• FDA 21 CFR Part 11 requirements
• Electronic Records and Electronic Data Management

Required Skills

Applicants should demonstrate:

• Good knowledge of Medical Terminology
• Strong communication skills
• Good writing and documentation skills
• Ability to work effectively in a team
• Ability to manage work within timelines
• Attention to detail
• Problem-solving and decision-making abilities

Educational Qualifications

According to the job description, candidates with the following educational backgrounds may be eligible:

Medical and Healthcare Qualifications

• BDS – Bachelor of Dental Surgery
• BAMS
• BHMS

Life Sciences and Pharmaceutical Qualifications

Candidates with a Master’s degree in any branch of Life Sciences or Pharmaceuticals may also be considered.

Additionally, the job description mentions:

• Diploma in Clinical Research

Relevant educational backgrounds and clinical research knowledge can strengthen a candidate’s application for this Clinical Data Management and data validation role.

Experience Required

The job listing indicates approximately 1 year of experience.

Candidates with relevant exposure to:

• Clinical Data Management
• Clinical Research
• Clinical Trials
• Data Validation
• EDC Systems
• Query Management
• CRF Review
• Database Testing
• Quality Control

may find this opportunity particularly relevant.

Why Consider a Career as a Validation Associate?

A Validation Associate role can provide practical exposure to important areas of the clinical research industry. Professionals in this role may gain experience with clinical databases, data validation procedures, query management, CRFs, edit checks, and reconciliation activities.

The role can help candidates develop knowledge in areas such as:

• Clinical Data Management (CDM)
• Electronic Data Capture (EDC)
• Clinical Trial Data
• Data Quality Management
• Query Management
• SAE Reconciliation
• Laboratory Data Reconciliation
• Good Clinical Practice
• Regulatory Compliance

For candidates interested in long-term careers in Clinical Data Management, this type of role can provide relevant operational experience.

Salary and Benefits

The job listing indicates a salary range of approximately ₹2–4 LPA.

Benefits may vary depending on company policies and employment terms. Candidates should confirm compensation, benefits, work arrangements, and other employment conditions during the recruitment process.

How to Apply

Application Link