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Clinical Research Associate Ii

2+ years
Not Disclosed
10 Aug. 22, 2024
Job Description
Job Type: Full Time Education: B.Pharm/ M.Pharm/ B.Sc/ M.Sc/ Any Life Science Graduate 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

About the Role: CRA II - Bangalore, India

Company: ICON plc

Location: Bangalore, India

Company Overview:

ICON plc is a leading global healthcare intelligence and clinical research organization. We are dedicated to fostering an inclusive environment that drives innovation and excellence in clinical development. Join us to be a part of our mission to shape the future of healthcare through cutting-edge research and development.

Role Overview:

We are seeking a Clinical Research Associate II Specialist to join our dynamic team in Bangalore. As a Clinical Research Associate II at ICON, you will be integral in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Key Responsibilities:

  • Site Management: Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Compliance and Data Integrity: Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaboration: Work closely with investigators and site staff to facilitate smooth study execution.
  • Data Management: Review data and resolve queries to maintain high-quality clinical data.
  • Documentation: Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Your Profile:

  • Education: Bachelor's degree in a scientific or healthcare-related field.
  • Experience: Minimum of 2 years as a Clinical Research Associate.
  • Knowledge: In-depth understanding of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Skills: Strong organizational and communication skills with keen attention to detail. Ability to work independently and collaboratively in a fast-paced environment.

What ICON Offers You:

At ICON, we value the quality of our people and are committed to creating a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, we offer a range of benefits designed to support your well-being and work-life balance:

  • Annual Leave: Various entitlements based on your location.
  • Health Insurance: A range of options to suit you and your family’s needs.
  • Retirement Planning: Competitive offerings to help you plan for the future.
  • Global Employee Assistance Programme: LifeWorks provides 24-hour access to a global network of professionals for support.
  • Life Assurance: Coverage for peace of mind.
  • Flexible Benefits: Country-specific options including childcare vouchers, bike purchase schemes, discounted gym memberships, and more.

Diversity and Inclusion:

ICON is an equal opportunity and inclusive employer. We are committed to a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Accommodation and Application:

If you require reasonable accommodation due to a medical condition or disability for any part of the application process, please let us know or submit a request here.

Interested in the Role?

Even if you don't meet all the requirements, we encourage you to apply. You might be exactly what we're looking for at ICON, whether for this role or other opportunities.

Current ICON Employees:

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