ICON plc Hiring for Clinical Data Coordinator II Role : Pharma Jobs 2026

Pharma Hiring Hub; Bengaluru; On-site; INR 600,000 - 1,200,000; Full time

Job summary

ICON plc is hiring a Clinical Data Coordinator II in Bengaluru. The role suits candidates with 1–3 years of clinical data management experience and a Life Sciences degree. You will support end-to-end data activities, ensure data quality, and collaborate with global project teams in a world-class CRO environment.

Expect involvement with eCRFs, data validation specs, and procedures, while working with Medidata Rave and Oracle RDC. Strong communication and cross‑functional teamwork are essential.

Qualifications

• Bachelor’s degree in Life Sciences or related field required.
• 1–3 years of clinical data management experience preferred.
• Familiarity with Medidata Rave, Oracle RDC or similar EDC systems.
• Strong communication and cross-functional collaboration skills.
• Irregularities awareness of ICH-GCP is a plus.

Responsibilities

• Assist Data Management Study Lead in maintaining study documents (eCRFs, Data Validation Specifications, Study Procedures).
• Perform reconciliation of clinical data with third‑party vendor data per edit check specs.
• Track study progress and share status with clinical data scientist and project teams.
• Address data‑related questions and propose effective solutions.
• Investigate data issues and support root-cause analyses to improve quality.

Skills

Attention to detail

Excellent communication

Cross-functional collaboration

Problem solving

Education

Bachelor’s degree in Life Sciences

M.Pharm

Lifescience Graduate

Tools

Medidata Rave

Oracle RDC

Job description

ICON plc, a globally recognized leader in clinical research and healthcare intelligence, is hiring a Clinical Data Coordinator II at its Bengaluru location. This role is ideal for candidates with 1–3 years of experience in clinical data management and a degree in Life Sciences. As a Data Coordinator II, you will support end‑to‑end clinical data activities, contribute to data quality checks, manage study documentation, and collaborate with global project teams, making it an excellent opportunity to advance your career in clinical data operations within a world‑class CRO.

Table of Contents

Job Overview

• Position: Clinical Data Coordinator II
• Department: CDM
• Location: Banglore
• Experience: 1 to 3 Years
• Qualification: B.Pharm, M.Pharm, Lifescience Graduate
• Job Type: Full-Time
• Last Date of application: 23 March 2026

Key Responsibilities – Clinical Data Coordinator II

• Assist the Data Management Study Lead in maintaining study documents such as eCRFs, Data Validation Specifications, and Study‑Specific Procedures to ensure smooth data management operations.
• Perform reconciliation of clinical data and third‑party vendor data in accordance with edit check specifications and data review plans, ensuring all datasets are consistent and accurate.
• Track study progress and task metrics, and share timely status updates with the clinical data scientist, project team, and functional managers.
• Address data‑related questions from internal and external teams, providing clear responses and recommending effective solutions.
• Investigate data issues, identify root causes, and support systematic resolution to improve data quality and prevent recurrence.

Required Skills & Qualifications

• A Bachelor’s degree in Life Sciences, Healthcare, or another relevant scientific discipline.
• Intermediate understanding of clinical data management processes, ideally gained within the pharmaceutical, biotechnology, or CRO industry.
• Familiarity with common data management systems such as Medidata Rave, Oracle RDC, or similar EDC platforms.
• Strong accuracy and focus when reviewing clinical data, identifying discrepancies, and supporting data quality activities.
• Excellent communication skills and the ability to work effectively with cross‑functional teams in a fast‑paced environment.
• Basic awareness of ICH‑GCP guidelines, regulatory expectations, and clinical trial documentation standards is an added advantage.

Why Join ICON plc?

• As a Clinical Data Coordinator II, you gain hands‑on experience with EDC systems, data reconciliation, validation checks, study documentation, and industry‑standard processes — helping you advance rapidly in your CDM career.
• ICON promotes a team‑driven environment where you collaborate with clinical data scientists, project managers, medical teams, and global stakeholders, ensuring continuous learning and professional growth.
• You’ll work with international clients and cutting‑edge data management technologies used across global clinical trials, enhancing both your technical and domain expertise.
• ICON offers structured training, mentorship, and cross‑functional exposure, preparing you for future roles such as Senior Data Coordinator, Lead Data Manager, or Clinical Data Scientist.
• Every task you perform contributes directly to improving data quality in clinical trials, ultimately helping bring safer and more effective treatments to patients worldwide.

1. What does a Clinical Data Coordinator II do at ICON?

ICON typically requires 1–3 years of experience in clinical data management or a related clinical research function.

2. What experience is required for this role?

ICON typically requires 1–3 years of experience in clinical data management or a related clinical research function.

3. What educational background is needed?

A Bachelor’s degree in Life Sciences, Healthcare, or a related scientific discipline is required.

4. Do I need experience with EDC systems?

Yes. Familiarity with systems such as Medidata Rave, Oracle RDC, or similar EDC platforms is highly preferred.

5. Will I be working with global teams?

Yes. ICON is a global CRO, and you will collaborate with clinical data scientists, project managers, and cross‑functional teams across regions.