Role Overview
ICON is hiring a entry-level Clinical Research Associate II. This is a full-time role in IN. Part of ICON's Qa hiring, posted 5 days ago. Full responsibilities, required qualifications, and the apply link are listed in the description below.
Salary Context
Salary is not disclosed in this posting. Market median for Junior-level Qa roles is $70k-$96k (based on 34 comparable listings). Many employers share specifics during the interview process or after an initial screen.
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Job Description
As a Clinical Research Associate II at the worlds largest & most comprehensive clinical research organization in Mumbai, you will have the opportunity to work in a partnership-driven environment focused on innovation and continuous improvement. This role is ideal for individuals seeking a workplace where they feel a sense of belonging, are empowered to reach their full potential, perform at their best, and make a valuable contribution to saving lives.
- *Key Responsibilities:**
- Perform all aspects of CRA duties including site selection, site initiation, routine monitoring visits, and close-out visits
- Work closely with our client's study team and have a dedicated ICON line manager for support
- Oversee study site management to ensure high-quality data with low query levels and good Quality Assurance reports
- Support and mentor other team members
- *Qualifications Required:**
- Education: B.Pharm/M.Pharm/Pharm D/BDS/MBBS
- Minimum 2 years of onsite monitoring experience in Oncology (excluding training & induction)
- Strong and clear communication skills
(Note: No additional details about the company were provided in the job description) As a Clinical Research Associate II at the worlds largest & most comprehensive clinical research organization in Mumbai, you will have the opportunity to work in a partnership-driven environment focused on innovation and continuous improvement. This role is ideal for individuals seeking a workplace where they feel a sense of belonging, are empowered to reach their full potential, perform at their best, and make a valuable contribution to saving lives.
- *Key Responsibilities:**
- Perform all aspects of CRA duties including site selection, site initiation, routine monitoring visits, and close-out visits
- Work closely with our client's study team and have a dedicated ICON line manager for support
- Oversee study site management to ensure high-quality data with low query levels and good Quality Assurance reports
- Support and mentor other team members
- *Qualifications Required:**
- Education: B.Pharm/M.Pharm/Pharm D/BDS/MBBS
- Minimum 2 years of onsite monitoring experience in Oncology (excluding training & induction)
- Strong and clear communication skills
(Note: No additional details about the company were provided in the job description)
About ICON
ICON
iconplc.com
2 other open roles at ICON on TryApplyNow.
Frequently Asked Questions
How do I apply for the Clinical Research Associate II position at ICON?
Use the Apply button above to submit your application directly to ICON. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Clinical Research Associate II position at ICON located?
This position is based in IN. ICON has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a Clinical Research Associate II at ICON earn?
ICON has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the Clinical Research Associate II role at ICON posted?
This role was posted on June 25, 2026 (5 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
Is the Clinical Research Associate II role at ICON entry-level?
Yes. This is an entry-level position. Strong candidates typically have 0-2 years of relevant work experience, internships, or significant project work. Read the full description for any specific qualification requirements ICON has listed.
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