Parexel Hiring In House Clinical Research Associate in Bengaluru for clinical trial start-up, regulatory submissions, and site management roles.
Parexel has announced a verified full-time opportunity for the position of iCRA II (In-House Clinical Research Associate II) at its Bengaluru, India location. This role is part of Parexel’s global clinical operations team and plays a critical role in clinical trial start-up, regulatory submissions, site activation, and ongoing trial maintenance.
This position is ideal for experienced clinical research professionals with strong start-up and regulatory experience, solid knowledge of ICH-GCP, and the ability to manage multiple stakeholders across global clinical trials. Parexel Hiring In House Clinical Research
About the Company
Parexel is a leading global clinical research organization (CRO) dedicated to improving world health. From early-phase clinical trials to regulatory consulting and market access, Parexel provides comprehensive clinical development solutions to pharmaceutical, biotechnology, and medical device companies.
What sets Parexel apart is its strong patient-first philosophy. Every role at Parexel directly or indirectly contributes to the development of therapies that benefit patients worldwide. The organization promotes a culture of empathy, quality, collaboration, and accountability, empowering employees to make a meaningful difference in global healthcare. Parexel Hiring In House Clinical Research
Job Details
Company Name: Parexel
Job Title: iCRA II (In-House Clinical Research Associate II)
Job Requisition ID: R0000036655
Job Location: Bengaluru, India
Employment Type: Full-time | Permanent
Industry: Clinical Research / CRO
Application Deadline: January 19, 2026
Job Description
The iCRA II role at Parexel is a critical operational position responsible for managing clinical trial activities from site identification through site close-out, with a strong focus on study start-up and regulatory compliance. Parexel Hiring In House Clinical Research
As an iCRA II, you will act as Parexel’s primary point of contact for assigned clinical sites, ensuring high-quality delivery, regulatory readiness, and compliance with global and local requirements. You will work closely with investigators, site staff, sponsors, internal project teams, and regulatory authorities to ensure smooth site activation and ongoing trial execution.
This role requires a self-driven professional who can work with minimal supervision, proactively manage risks, and maintain high standards of quality and documentation. Parexel Hiring In House Clinical Research
Key Responsibilities
Study Start-Up (Site Identification to Activation)
- Act as Parexel’s primary contact for assigned sites during the start-up phase
- Build and maintain strong relationships with investigators and site staff
- Support country-specific feasibility, site pre-qualification, and qualification activities
- Prepare, negotiate, and facilitate execution of Confidentiality Agreements (CDAs) and amendments
- Conduct remote Qualification Visits (QVs) when required
- Liaise with stakeholders to understand and manage Clinical Site Agreement (CSA) timelines
- Manage country and site-level TMF documentation, ensuring First Time Quality (FTQ)
- Develop strategies for collecting, reviewing, approving, and maintaining essential regulatory documents
- Customize, review, and negotiate Informed Consent Forms (ICFs) and translations as per country and regulatory requirements
- Prepare and submit IRB/IEC and MoH/Regulatory Authority (RA) applications and follow up until final approval
- Ensure timely submission of all documents to the Trial Master File (TMF)
- Maintain and update Clinical Trial Management Systems (CTMS) accurately and on time
Study Maintenance (Initiation to Close-Out)
- Manage amendments to ICFs and regulatory submissions during trial maintenance
- Prepare and submit ongoing IRB/IEC and MoH/RA applications as required
- Track regulatory approvals and timelines and update trial systems accordingly
- Ensure all trial documentation is filed in TMF as per sponsor and company policies
Overall Trial Responsibilities (Start-Up to Close-Out)
- Ensure timely and accurate completion of project milestones
- Maintain audit- and inspection-ready sites at all times
- Monitor compliance with ICH-GCP, local, and international regulations
- Identify, resolve, or escalate site-related risks including delays, training gaps, data quality concerns, or compliance issues
- Support site access to study systems and ensure completion of required trainings
- Participate in internal and external meetings as per project needs
- Work collaboratively with global and local teams to achieve project goals
- Proactively communicate progress, risks, and issues to line management
- Support junior team members and act as a mentor and role model
- Complete administrative tasks such as timesheets, metrics, and expenses on time
Parexel Hiring In House Clinical Research
Skills & Competencies
Core Skills
- Strong problem-solving and analytical abilities
- Excellent stakeholder and client management skills
- Ability to work independently with minimal supervision
- Strong decision-making skills in ambiguous and fast-changing situations
- Ability to manage multiple priorities and tight timelines
- Excellent written, verbal, and interpersonal communication skills
- High attention to detail and commitment to quality
- Ability to work effectively in global, cross-cultural, and virtual teams
Parexel Hiring In House Clinical Research
Technical Skills
- Strong working knowledge of CTMS, eTMF, and MS Office (Excel, Word)
- Understanding of clinical trial documentation and regulatory processes
- Familiarity with ICH-GCP guidelines and clinical research terminology
Parexel Hiring In House Clinical Research
Education & Experience
Education
- Bachelor’s degree in Biological Sciences, Pharmacy, or other health-related discipline preferred
- Nursing qualification or equivalent clinical research experience will also be considered
Experience
- Substantial clinical trial start-up experience or equivalent experience in clinical research
- Strong understanding of clinical trial methodology, regulatory submissions, and site management
Parexel Hiring In House Clinical Research
Benefits & Work Culture
Parexel offers a supportive and performance-driven work environment with benefits aligned to global CRO standards:
- Permanent, full-time role in a global CRO
- Exposure to international clinical trials and sponsors
- Strong learning and career development opportunities
- Collaborative and patient-focused culture
- Opportunity to grow as a subject matter expert in clinical start-up and operations
Why You Should Join
Joining Parexel as an iCRA II means becoming part of an organization where values, quality, and patient impact are at the center of everything. This role offers deep exposure to clinical trial start-up, regulatory strategy, and site management, making it a strong career move for professionals aiming to advance in clinical operations.
If you are passionate about clinical research, thrive in a dynamic global environment, and want to contribute to therapies that improve lives, Parexel provides the platform to achieve your career goals. Parexel Hiring In House Clinical Research
FAQs
Is this a permanent role?
Yes, this is a full-time, permanent position.
Where is the job located?
The role is based in Bengaluru, India.
Is start-up experience mandatory?
Yes, substantial start-up or equivalent clinical research experience is required.
What systems will I work with?
CTMS, eTMF, and other clinical trial systems.
What is the last date to apply?
January 19, 2026.
Parexel Hiring In House Clinical Research
How to Apply
Interested candidates should apply online through the official Parexel careers portal using: Parexel Hiring In House Clinical Research
Job Requisition ID: R0000036655
This is a strong opportunity to grow your clinical research career with Parexel in Bengaluru.
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