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 Analyst (Data Manager, Clinical Operations Analyst) to join our team in a hybrid / on-site capacity. As a Clinical Data Analyst, you will support clinical research activities that advance new treatments for patients. This position plays a key role in study execution, data integrity oversight, regulatory compliance, and clinical data accuracy. You'll collaborate with cross-functional teams, follow industry-standard processes, and contribute to study operations from planning through database lock.
Responsibilities include managing clinical data review workflows, resolving data discrepancies, and ensuring data quality through systematic query management and vendor reconciliation. With diverse teams and continuous learning opportunities, the Clinical Data Analyst can explore career paths and expand skills across clinical data management, regulatory affairs, and clinical operations.
Key Responsibilities
- Conduct comprehensive clinical data reviews and data cleaning activities to ensure accuracy, completeness, and compliance with study protocols and regulatory requirements
- Review clinical data listings and identify discrepancies, inconsistencies, and data quality issues requiring resolution
- Manage query workflows, including query generation, tracking, resolution, and documentation to support timely database closure
- Perform vendor data reconciliation activities, including local laboratory data review and external data verification to ensure data integrity
- Execute CRF freeze and lock activities in accordance with study timelines and regulatory standards, coordinating with clinical sites and internal teams
- Conduct User Acceptance Testing (UAT) for data listings, system screens, and edit checks to validate system functionality and data accuracy
- Maintain comprehensive study documentation within Veeva Vault and eTMF systems, ensuring proper organization, version control, and regulatory compliance
- Collaborate with cross-functional stakeholders including clinical monitors, programmers, biostatisticians, and regulatory teams to resolve data issues and support study milestones
- Demonstrate proficiency with clinical data workbench tools and EDC systems to support efficient data management and analysis
You'll thrive in this role if you bring:
- Strong expertise in clinical data review, data cleaning, and query management processes
- Hands-on experience with EDC systems and clinical data analysis tools in a fast-paced environment
- Proficiency with Veeva Vault, eTMF documentation systems, and clinical data workbench platforms
- Experience working in clinical research, healthcare, or a regulated environment with attention to regulatory compliance
- The ability to collaborate across teams and communicate clearly with internal and external stakeholders
- A patient-focused mindset and exceptional attention to detail in managing complex clinical datasets
- Comfort working with multiple software systems and a commitment to continuous learning
Required Qualifications
- Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related scientific discipline
- Minimum 2+ 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
- Working knowledge of clinical research regulations, GCP guidelines, and clinical trial processes
- Knowledge of ICH-GCP, regulatory requirements, and 21 CFR Part 11 compliance
- Strong communication, organization, and problem-solving skills
Preferred Qualifications
- Experience with data review tools such as J-Review or Spotfire
- Proficiency with Microsoft Project and advanced PowerPoint presentations
- Experience in vendor reconciliation and database lock activities
- Familiarity with clinical trial data management best practices and quality assurance processes
Skills Required
- Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related scientific discipline
- Minimum 2+ 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
- 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.
-
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.
-
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.
-
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.
