Parexel Hiring iCRA II Clinical Research Associate Jobs startup role global trials CRO career opportunity 2026 apply now.
Parexel has announced a new opportunity for experienced clinical research professionals with openings for the role of iCRA II (Initiation Clinical Research Associate) in Bengaluru. This position is focused on study start-up, site activation, and regulatory coordination activities within global clinical trials. The role is ideal for candidates with strong clinical trial start-up experience and a solid understanding of regulatory and site management processes.
Professionals aiming to build careers in clinical operations and CRA pathways within global CRO environments can explore this opportunity. The role offers direct involvement in site activation strategies, regulatory documentation, and cross-functional clinical trial execution. Parexel Hiring iCRA II Clinical Research Associate Jobs
Company Overview
Parexel is a leading global clinical research organization offering services across clinical development, regulatory consulting, and post-marketing support. The company partners with pharmaceutical and biotechnology sponsors to accelerate clinical trials and bring new therapies to patients worldwide.
With extensive global operations and diverse therapeutic exposure, Parexel provides strong career growth opportunities for clinical research professionals across multiple domains including monitoring, project leadership, and regulatory consulting. Parexel Hiring iCRA II Clinical Research Associate Jobs
Job Location & Employment Type
- Location: Bengaluru, India
- Employment Type: Full-time
- Department: Clinical Operations
- Role Type: Study Start-up / Initiation CRA
This role may involve collaboration with global teams and multi-region clinical studies. Parexel Hiring iCRA II Clinical Research Associate Jobs
Job Role Overview
The iCRA II will primarily focus on pre-study initiation and site activation activities. The role involves managing start-up deliverables from site identification through activation, ensuring regulatory readiness, and supporting ongoing site compliance throughout the study lifecycle.
This position requires expertise in clinical trial start-up, regulatory documentation, and strong stakeholder coordination skills. Parexel Hiring iCRA II Clinical Research Associate Jobs
Key Roles & Responsibilities
Study Start-Up & Site Activation
- Acting as the primary contact for assigned clinical trial sites during start-up
- Managing site activation timelines and regulatory readiness
- Supporting feasibility and site qualification activities
- Coordinating confidentiality agreements and site documentation
Regulatory & Documentation Management
- Preparing and submitting IRB/IEC applications and regulatory documentation
- Managing country-specific informed consent documentation
- Ensuring regulatory submissions are completed accurately and on time
- Maintaining trial master file (TMF) documentation quality
Site Relationship & Coordination
- Building strong relationships with investigators and site teams
- Supporting training and system access readiness
- Managing site queries and resolving start-up challenges
- Participating in internal and external project meetings
Parexel Hiring iCRA II Clinical Research Associate Jobs
Trial Systems & Compliance
- Updating clinical trial management systems (CTMS) regularly
- Ensuring inspection readiness of assigned sites
- Maintaining compliance with ICH-GCP and local regulations
- Monitoring documentation quality and completeness
Ongoing Study Maintenance
- Supporting amendments and regulatory updates during study lifecycle
- Managing informed consent updates where required
- Ensuring continuous compliance and documentation accuracy
- Supporting close-out readiness and project completion
This role requires structured project execution and strong ownership of start-up deliverables. Parexel Hiring iCRA II Clinical Research Associate Jobs
Eligibility Criteria
Educational Qualification
Candidates must hold a degree in a relevant healthcare or science discipline, such as:
- Life Sciences
- Pharmacy
- Nursing or healthcare-related qualifications
- Equivalent clinical research education
Candidates with clinical or regulatory academic backgrounds may have an advantage. Parexel Hiring iCRA II Clinical Research Associate Jobs
Experience
- Strong experience in clinical trial start-up or site activation
- Prior experience in CRO environments preferred
- Understanding of clinical trial methodology and terminology
- Experience with regulatory submissions and site coordination
Candidates with CRA or start-up specialist backgrounds are ideal for this role.
Skills Required
- Strong problem-solving and decision-making abilities
- Excellent communication and stakeholder management skills
- Ability to manage multiple timelines and deliverables
- Knowledge of CTMS, eTMF, and clinical systems
- Understanding of ICH-GCP guidelines
- Strong attention to detail and documentation quality
- Ability to work in matrix and global environments
Candidates with leadership potential and independent working ability may thrive in this role. Parexel Hiring iCRA II Clinical Research Associate Jobs
Salary & Benefits
- Compensation will be as per company norms and experience level
- Opportunity to work on global clinical trials
- Exposure to multi-region regulatory frameworks
- Career progression into CRA and clinical leadership roles
- Structured learning within a global CRO environment
This role offers strong long-term growth within clinical research operations.
Selection Process
The recruitment process may include:
- Resume screening based on CRA or start-up experience
- Functional or technical interview
- Final HR or leadership discussion
Candidates with strong start-up and regulatory experience may be prioritized.
How to Apply
Interested candidates can apply through the official Parexel careers portal by searching:
Role: iCRA II
Location: Bengaluru
Ensure your resume highlights:
- Clinical trial start-up experience
- Regulatory submission exposure
- CRO or global trial experience
- CTMS and TMF handling experience
Early applications are recommended due to high demand for CRA roles.
Important Dates
- Application Mode: Online application
- Hiring Type: Immediate / ongoing recruitment
Candidates are encouraged to apply early as roles may close after shortlisting.
Why Apply for This Pharma Job?
CRA roles remain among the most sought-after career paths in clinical research due to strong global demand and structured career progression. This iCRA II role provides specialized exposure to study start-up and activation processes, which are critical phases in clinical trials.
Professionals working in start-up roles often progress into Senior CRA, Clinical Trial Manager, or Project Leadership positions. The role also provides international regulatory exposure, which enhances long-term global career opportunities.
For clinical research professionals looking to advance within CRO environments, this opportunity offers a strong pathway into higher-level clinical operations roles. Parexel Hiring iCRA II Clinical Research Associate Jobs
Important Note
IndiaPharmaJobs.in is an independent pharmaceutical job information platform and is not affiliated with Parexel. We do not participate in the recruitment process. Applicants should apply through the official careers portal and verify job details independently before proceeding. Parexel Hiring iCRA II Clinical Research Associate Jobs
Final Words
If you have experience in clinical trial start-up or CRA roles and want to grow within a global CRO, this iCRA II opportunity at Parexel is worth considering. With exposure to site activation, regulatory submissions, and global clinical trial environments, the role provides strong career advancement potential. Apply early and ensure your resume highlights relevant start-up and regulatory expertise for better shortlisting chances. Parexel Hiring iCRA II Clinical Research Associate Jobs
