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Hybrid Clinical Data Management Job at ICON plc, India | Medical Professionals Are Welcome!

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Hybrid Clinical Data Management Job at ICON plc, India. Medical Professionals Apply for this CDC Role at ICON plc Careers.

Hybrid Clinical Data Management Job at ICON plc

Are you ready to embark on a journey with ICON plc, a leader in healthcare intelligence and clinical research? This hybrid clinical data management job offers a unique opportunity to work at the forefront of the pharmaceutical and biotechnology sectors. Located in Bangalore, Chennai, Trivandrum, and Bengaluru, this role is perfect for professionals with a passion for clinical data and a drive to contribute to innovative treatments and therapies. ICON plc is actively seeking talented individuals to join their dynamic team. If you’re eager to make a significant impact in clinical research, this position might be your next career milestone.

About ICON plc:

ICON plc is a world-leading healthcare intelligence and clinical research organization operating in the pharmaceutical and biotechnology sectors. With a commitment to fostering an inclusive environment, ICON is dedicated to driving innovation and excellence in clinical development. The organization is headquartered in Dublin, Ireland, and has a significant presence in India, where it is actively seeking talent for various roles, including the clinical data management job.

Job Details:

  • Job Title: Clinical Data Coordinator
  • Job Reference: JR156089
  • Location: Bangalore, Chennai, Trivandrum, Bengaluru
  • Job Type: Hybrid
  • Department: ICON Strategic Solutions (FSP)

Clinical Data Management Job Description:

As a Clinical Data Coordinator I at ICON, the selected candidate will design and analyze clinical trials, interpreting complex medical data to contribute to the advancement of innovative treatments and therapies. This hybrid clinical data management job requires a blend of technical expertise and communication skills to ensure the successful delivery of clinical research projects.

Key Responsibilities:

  • Assist the Data Management Study Lead in the development of eCRF, Data Validation Specifications, and Study-Specific Procedures.
  • Review clinical and third-party data based on edit specifications and data review plans.
  • Issue clear, accurate, and concise queries to investigational sites.
  • Communicate effectively with peers, clinical data scientists, and functional management.
  • Perform other project activities to ensure that study timelines are met, including filing and archiving study documentation.

Eligibility Criteria for the Clinical Data Management Job:

The ideal candidate will possess relevant clinical research experience along with the following qualifications:

  • Bachelor’s degree in a relevant field, such as Healthcare.
  • Basic 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.

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