Clinical Data Coordinator Hiring at Icon Plc

Clinical Data Coordinator I – Life Sciences, Bengaluru

Apply for Clinical Data Coordinator I at ICON, Bengaluru, Trivandrum, Chennai. Life Sciences grads with data management knowledge eligible.

ICON plc, a global leader in healthcare intelligence and clinical research, is inviting applications for the role of Clinical Data Coordinator I in Bengaluru, Trivandrum, and Chennai. This role provides an opportunity to contribute to innovative clinical trials, ensuring high-quality data management and supporting the development of groundbreaking medical therapies.

Company Overview

ICON plc is a premier clinical research organization and healthcare intelligence provider dedicated to advancing global healthcare. With expertise across multiple therapeutic areas, ICON leverages cutting-edge technologies and a highly skilled workforce to deliver accurate clinical trial data and actionable insights. The company fosters an inclusive, innovative, and collaborative environment, making it a sought-after workplace for life sciences professionals.

Job Role & Responsibilities

As a Clinical Data Coordinator I at ICON, your responsibilities will include:

• Assisting Data Management Study Leads in the development of electronic Case Report Forms (eCRF), Data Validation Specifications, and Study-Specific Procedures.
• Reviewing clinical and third-party data according to edit specifications and data review plans.
• Issuing clear, accurate, and concise queries to investigational sites.
• Communicating effectively with peers, clinical data scientists, and functional management as required.
• Performing project activities to ensure study timelines are met, including filing and archiving study documentation.
• Dispatching queries to investigator sites for resolution and tracking progress.
• Supporting cross-functional teams to maintain the integrity and quality of clinical trial data.

Eligibility / Qualifications

• Educational Background: Bachelor’s degree in Life Sciences or Healthcare.
• Experience: Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry.
• Familiarity with data management software and systems such as Medidata, Oracle RDC, or similar platforms.
• Strong attention to detail and the ability to work in a fast-paced environment.
• Excellent communication and collaboration skills.
• Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is an added advantage.

Relevant Courses: B. Pharma, BSc Life Sciences, Biotechnology, Microbiology, Nursing, Medical Laboratory Sciences, M. Pharma, MSc Life Sciences, PG Diploma in Clinical Research.

Location & Salary

Locations: Bengaluru, Trivandrum, Chennai, India (Office-based role)
Salary: Not disclosed; competitive and commensurate with experience.

Application Process

Interested candidates can apply via the ICON careers portal: Apply Here. Early applications are encouraged due to the competitive nature of the role.

FAQs

Q1: What is the required experience for this role?
A1: Candidates should have basic knowledge of clinical data management within pharmaceutical or biotechnology industries.

Q2: What educational qualifications are required?
A2: A Bachelor’s degree in Life Sciences or Healthcare is required.

Q3: Where are the job locations?
A3: Bengaluru, Trivandrum, and Chennai, India.

Q4: What are the primary responsibilities of the Clinical Data Coordinator I?
A4: Developing eCRFs, reviewing clinical data, issuing queries to sites, performing data management tasks, and ensuring adherence to study timelines.

Q5: Is knowledge of regulatory standards necessary?
A5: Knowledge of ICH-GCP or similar regulatory standards is beneficial.

Q6: How can I apply for this position?
A6: Apply directly through the ICON careers link provided above with an updated CV.

Join ICON as a Clinical Data Coordinator I and play a critical role in the success of clinical trials, contributing to innovative treatments and the advancement of healthcare globally.

Tagged as: Pharma Jobs in Bangalore