Leading global clinical research organization ICON is currently hiring for the position of CRA II – Oncology (Phase III) in Hyderabad. This opportunity is ideal for experienced Clinical Research Associates seeking to advance their careers in oncology clinical trials and global drug development programs.
Candidates with strong experience in Phase III Oncology trials, site monitoring, and ICH-GCP compliance are encouraged to apply. Professionals available to join immediately or within 60 days will be given preference.
About ICON
ICON plc is a leading global healthcare intelligence and clinical research organization providing outsourced development and commercialization services to pharmaceutical, biotechnology, medical device, and government organizations worldwide. The company supports innovative clinical research programs that improve patient outcomes globally.
Job Details
| Particulars | Details |
|---|---|
| Job Title | CRA II – Oncology |
| Company | ICON |
| Location | Hyderabad, Telangana |
| Experience | 2+ Years |
| Industry | Clinical Research |
| Therapeutic Area | Oncology |
| Trial Phase | Phase III |
| Employment Type | Full-Time |
| Joining Preference | Immediate to 60 Days |
Key Responsibilities
As a CRA II – Oncology, you will:
- Conduct onsite monitoring visits for Phase III oncology clinical trials.
- Ensure compliance with ICH-GCP, protocol requirements, and regulatory guidelines.
- Monitor patient safety, data quality, and site performance.
- Review source documents and verify clinical trial data accuracy.
- Maintain effective communication with investigators and site staff.
- Support site initiation, routine monitoring, and closeout activities.
- Manage site documentation and regulatory submissions.
- Identify and resolve site-related issues proactively.
- Ensure timely reporting and completion of monitoring activities.
Required Qualifications
Candidates should possess:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or related healthcare disciplines.
- Minimum 2 years of experience as an Onsite Clinical Research Associate (CRA).
- Strong monitoring experience in Phase III Oncology clinical trials.
- Good understanding of clinical trial regulations and ICH-GCP guidelines.
- Experience with site management and investigator interactions.
- Ability to travel for monitoring visits as required.
- Strong communication and documentation skills.
Preferred Skills
- Global clinical trial experience.
- Experience working with multinational sponsors.
- Knowledge of oncology protocols and therapeutic area requirements.
- Strong problem-solving and risk management capabilities.
- Familiarity with electronic clinical trial systems and databases.
Why Join ICON?
- Work on cutting-edge oncology clinical trials.
- Exposure to global clinical research programs.
- Competitive compensation and benefits package.
- Career growth opportunities within a leading CRO.
- Collaborative and diverse work environment.
- Opportunity to contribute to innovative cancer therapies.
How to Apply
Interested candidates can share their updated CV or referrals directly to:
Email: kavitha.k@iconplc.com
Applicants who meet the eligibility criteria and can join within 60 days are encouraged to apply as soon as possible.
