Methics Hiring Clinical Data Coordinator

BPharm/MSc Clinical Data Coordinator Vacancy Valsad

BPharm/MSc Clinical Data Coordinator vacancy in Valsad. 2–4 years CDM experience required. Salary up to ₹4 LPA.

Clinical research organizations depend heavily on accurate, compliant, and well-managed clinical trial data to ensure patient safety, regulatory acceptance, and scientific credibility. Methics Clinical is currently expanding its clinical data management operations and is inviting experienced professionals to apply for the position of Clinical Data Coordinator at its Valsad, Gujarat office. This opportunity is ideal for candidates with hands-on Clinical Data Management (CDM) experience who want to work in a structured, compliance-driven research environment and contribute directly to high-quality clinical trial execution.

Company Overview

Methics Clinical is a growing clinical research organization delivering end-to-end clinical research services across multiple therapeutic areas. The organization supports sponsors, CROs, and research partners with robust clinical operations, data management, and regulatory-compliant processes aligned with global standards. With a strong focus on data integrity, regulatory adherence, and operational excellence, Methics Clinical plays a critical role in generating reliable clinical evidence that supports the development of safe and effective healthcare solutions.

The company follows internationally accepted guidelines including ICH-GCP, CDISC, and regulatory data standards, ensuring that all clinical trial data meets expectations of global health authorities. Professionals working at Methics Clinical gain exposure to real-world clinical datasets, cross-functional collaboration, and structured project workflows that enhance long-term career growth in clinical research.

Job Role & Responsibilities

The Clinical Data Coordinator will be responsible for managing and reviewing clinical trial data throughout the study lifecycle, from study start-up to database lock. This role requires strong technical knowledge of CDM processes, EDC systems, and regulatory standards.

Key Responsibilities

• Perform User Acceptance Testing (UAT) for screen designs and validation checks within EDC systems
• Prepare, review, and maintain Edit Specification Documents (ESD) and Data Validation Plans (DVP)
• Execute UAT for edit checks and document pass/fail test data
• Manage discrepancies including data review, verification, and reconciliation
• Prepare study-specific data management documents such as eCRF completion guidelines and test plans
• Assign and manage laboratory reference ranges within CDMS
• Conduct SAE, laboratory, and third-party data reconciliation activities
• Perform logical data review and ongoing data quality control checks
• Maintain and update project-specific trackers and timelines
• Supervise and review Master Data Management File documentation
• Support timely database lock and study close-out activities

This position demands precision, accountability, and a strong understanding of clinical data workflows, making it a high-value role within the clinical research domain.

Eligibility / Qualifications

Candidates applying for this role must meet the following requirements:

Educational Qualifications

• B.Pharm, M.Pharm, M.Sc (Life Sciences), Clinical Research, or related disciplines

Relevant courses include: B.Pharm, M.Pharm, M.Sc Clinical Research, M.Sc Life Sciences, PG Diploma in Clinical Data Management, PG Diploma in Clinical Research

Experience Requirements

• 2–4 years of hands-on Clinical Data Management experience
• Exposure to study start-up, conduct, and close-out phases
• Strong working knowledge of EDC systems
• Good understanding of ICH-GCP, CDISC standards, and clinical trial regulations
• Immediate joiners only

Location & Salary

• Job Location: Valsad, Gujarat (Office-based role)
• Annual Salary: Up to ₹4,00,000 per annum
• Work Mode: Full-time, on-site

The Valsad location offers a focused office environment suited for professionals looking to build stability and depth in clinical data management careers.

Application Process

Interested candidates who meet the experience, budget, and immediate joining criteria are encouraged to apply.

• Email your CV to: hr@methicsclinical.com
• Subject Line: Application for Clinical Data Coordinator – Valsad

Only shortlisted candidates will be contacted for further interview rounds.

Why Join Methics Clinical?

• Hands-on involvement in real clinical trial data
• Strong emphasis on data integrity and regulatory compliance
• Exposure to global clinical research standards
• Stable office-based role with structured processes
• Career growth in Clinical Data Management and Clinical Research Operations

Frequently Asked Questions (FAQs)

Is this role suitable for freshers?

No. This position requires 2–4 years of core Clinical Data Management experience.

Is remote or hybrid work available?

No. This is a fully office-based role in Valsad, Gujarat.

What type of studies will I work on?

Candidates will support multiple clinical studies involving EDC-based data management and reconciliation activities.

Is immediate joining mandatory?

Yes. Only immediate joiners will be considered for this position.

What are the growth opportunities?

This role offers long-term growth in CDM leadership, data quality oversight, and clinical operations coordination.

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Company	Methics Clinical
Vacancies	Clinical Data Coordinator
Required Education	B.Pharm, M.Pharm, M.Sc, Clinical Research
Experience	2–4 Years in Clinical Data Management