CDC II New

NetVerks Inc.; Chennai; On-site; INR 900,000 - 1,300,000; Full time

Benefits offered by this job

Health and wellbeing programmes

Retirement and pension plans

Learning and development opportunities

Job summary

ICON is seeking a Clinical Data Manager to work in a sponsor-dedicated model, contributing to the development of treatments. You will design and analyze clinical data, ensuring data quality and regulatory compliance, and collaborate with cross-functional teams.

The role involves maintaining eCRF and study procedures, data reconciliation, and guiding data-driven decisions in a fast-paced environment, with opportunities for career growth.

Qualifications

• Bachelor’s degree in Life Sciences or Healthcare.
• Experience in clinical data management within pharma/biotech.
• Familiarity with data management software (Medidata, Oracle RDC).
• Strong attention to detail in fast-paced environments.
• Excellent communication and cross-functional collaboration.
• Knowledge of ICH-GCP is a plus.

Responsibilities

• Deliver clinical data management work to a high standard with the team and stakeholders.
• Assist Study Lead in maintenance of eCRF, DVS, and Study Specific Procedures.
• Manage data reconciliation with edit specifications and data review plans.
• Track and communicate status of study metrics to data scientist and management.
• Identify root causes to resolve data issues.

Skills

Data management

eCRF maintenance

Attention to detail

Cross-functional collaboration

ICH-GCP knowledge

Education

Bachelors in Life Sciences / Healthcare

Tools

Medidata

Oracle RDC

Job description

CDC IIAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

CDC IIAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do

Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.

Key responsibilities include

• Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
• Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
• Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.
• Address data related questions and recommend potential solutions.
• Identify root cause to systematically resolve data issues.

Your Profile

You will bring relevant clinical data management experience, along with the following qualifications and skills.

Required qualifications and experience

• Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
• Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
• Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
• Strong attention to detail and the ability to work effectively in a fast-paced environment.
• Excellent communication skills and the ability to collaborate with cross-functional teams.
• Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.