When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About ParexelParexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose – moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®.
About the Role
We are seeking a Clinical Data Management II to join our team in India on hybrid capacity. As a Clinical Data Management Associate, you will support clinical trial data review, data cleaning, and query management activities that advance new treatments for patients. This position plays a key role in ensuring data integrity, regulatory compliance, and clinical data accuracy. You'll collaborate with cross-functional teams including clinical monitors, EDC vendors, and regulatory specialists, follow industry-standard processes, and contribute to study operations from data entry through database lock and closeout.
Responsibilities include conducting comprehensive clinical data reviews, managing data discrepancies, performing CRF freeze and lock activities, and coordinating vendor data reconciliation, with opportunities to deepen your expertise in clinical data management and influence study outcomes.
You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through rigorous data stewardship, quality assurance, and cross-functional collaboration. With diverse teams and continuous learning opportunities, the Clinical Data Management Associate can explore career paths and expand skills across clinical research and data management.
Key Responsibilities
- Conduct comprehensive clinical data reviews using EDC systems and data review tools to identify discrepancies, missing data, and protocol deviations
- Manage data queries, track discrepancy resolution, and coordinate with clinical sites and internal stakeholders to ensure timely and accurate data corrections
- Perform CRF freeze and lock activities, including validation of data completeness and accuracy prior to database lock
- Reconcile vendor-supplied data, including local laboratory results and external data sources, ensuring alignment with EDC data and source documentation
- Conduct User Acceptance Testing (UAT) for EDC listings, screens, and edit checks to validate system functionality and data integrity
- Maintain comprehensive study documentation within eTMF and Veeva Vault systems, ensuring compliance with regulatory requirements and company standards
- Collaborate with cross-functional teams including clinical monitors, data managers, EDC vendors, and regulatory specialists to support study execution and data quality
- Communicate data quality issues, discrepancies, and resolutions clearly to stakeholders through written reports and team meetings
You'll thrive in this role if you bring:
- Strengths in clinical data review, attention to detail, and problem-solving in complex data environments
- Hands-on experience with EDC systems, data review tools, and clinical data management processes
- The ability to collaborate across teams and communicate clearly with clinical sites, vendors, and internal stakeholders
- A patient-focused mindset, strong attention to detail, and commitment to data integrity and regulatory compliance
- Comfort working with EDC systems, data review platforms, eTMF documentation systems, and Microsoft Office Suite
- Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related scientific discipline
- Minimum 4+ years of experience in Clinical Data Management within a CRO, pharmaceutical, or biotechnology environment
- Hands-on experience with EDC systems, preferably Medidata RAVE and Oracle Clinical
- Experience in data review, query management, vendor reconciliation, and database lock activities
- Knowledge of ICH-GCP, regulatory requirements, 21 CFR Part 11, and clinical trial processes
- Strong communication, organization, and problem-solving skills
Preferred Qualifications
- Experience with Veeva Vault and eTMF documentation systems
- Familiarity with data review tools such as J-Review or Spotfire
- Experience with Clinical Data Workbench or other advanced data analysis platforms
- Experience in specific therapeutic areas or study phases
If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply!
We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.
Skills Required
- Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related scientific discipline
- Minimum 4+ years of Clinical Data Management experience within a CRO, pharmaceutical, or biotechnology environment
- Hands-on experience with EDC systems
- Experience with Medidata RAVE and Oracle Clinical
- Experience in clinical data review, query management, vendor reconciliation, and database lock activities
- Working knowledge of clinical research regulations, GCP guidelines, and clinical trial processes
- Experience with Veeva Vault and eTMF documentation
Parexel Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Parexel and has not been reviewed or approved by Parexel.
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Healthcare Strength — Health coverage is described as comprehensive, including medical, dental, vision, HSA/FSA options, and company-paid disability insurance. Descriptions often portray the package as strong or “top notch,” adding meaningful value.
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Retirement Support — Retirement offerings include a 401(k) with company matching and, in some regions, generous pension contributions. Core financial protections are emphasized as a solid part of the total rewards.
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Leave & Time Off Breadth — Time-off programs include ample PTO or flexible/unlimited RTO alongside flexible schedules and remote/hybrid options. Work-life balance support from managers is highlighted as a practical advantage.
Parexel Insights
What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
