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Cdc Ii

2+ years
Not Disclosed
10 Oct. 30, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Data Coordinator II - Trivandrum/Chennai, India (Office-Based)

Company: ICON plc

About Us: ICON plc is a leading healthcare intelligence and clinical research organization dedicated to fostering an inclusive environment that drives innovation and excellence. We invite you to join us on our mission to shape the future of clinical development!

Position Overview: We are seeking a Clinical Data Coordinator II to become a key member of our dynamic team. In this role, you will assist in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Key Responsibilities:

  • Assist the Data Management Study Lead in maintaining electronic Case Report Forms (eCRF), Data Validation Specifications, and Study-Specific Procedures.
  • Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
  • Track and communicate the status of study and task metrics to clinical data scientists, project teams, and functional management.
  • Address data-related questions and recommend potential solutions.
  • Identify root causes and systematically resolve data issues.

Qualifications:

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

What ICON Can Offer You: Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. Alongside a competitive salary, ICON provides a comprehensive benefits package focused on well-being and work-life balance, including:

  • Various annual leave entitlements.
  • A range of health insurance offerings to meet you and your family’s needs.
  • Competitive retirement planning options.
  • Global Employee Assistance Programme for 24-hour support.
  • Life assurance and flexible optional benefits.

To learn more about our benefits, visit our careers site.

Diversity and Inclusion: ICON is an equal opportunity and inclusive employer committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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

Interested but Unsure? If you’re interested in this role but don’t meet all the requirements, we encourage you to apply—there’s a chance you might be exactly what we’re looking for!

Current ICON Employees: If you are a current ICON employee, please click here to apply.