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Full-time
bachelor degree
Posted 1d ago
~40 hrs/week
Responsibilities
The Clinical Data Analyst will support data cleaning, study build activities, vendor reconciliations, and database lock processes for global clinical trials. They will also manage data discrepancies, conduct UAT activities, and collaborate with cross-functional teams to ensure high-quality study delivery.
Requirements
Candidates must have at least 4 years of experience in clinical data management and proficiency with EDC systems like Medidata Rave. A Bachelor's degree in Life Sciences, Pharmacy, or a related field is required, along with strong knowledge of ICH-GCP guidelines.
Full job description
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.
Job Summary
We are seeking an experienced Clinical Data Analyst with 4+ years of clinical data management experience to support data review, data cleaning, study build activities, vendor reconciliations, and database lock processes across global clinical trials. The role will be responsible for reviewing clinical data listings, managing data discrepancies, supporting CRF (Case Report Forms) and edit check development, conducting UAT (User Acceptance Testing) activities, reviewing complex external data sources, and ensuring compliance with GCP and regulatory requirements. The successful candidate will collaborate with cross-functional teams, mentor junior CDM (Clinical Data Management) staff, and contribute to high-quality study delivery across therapeutic areas such as Oncology, Hematology, Cardiovascular, Fibrosis, and Cell Therapy.
Skillsets
Minimum 4+ years of experience in Clinical Data Review and Clinical Data Management.
Hands-on experience with Medidata RAVE and other EDC (Electronic Data Capture) systems.
Experience supporting study build activities, including CRF design, edit checks, and integrations.
Experience performing UAT during study build and validation phases.
Strong experience in vendor reconciliation and external data review.
Experience with database lock activities, including CRF freeze and lock processes.
Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
Experience working within Veeva Vault and eTMF environments.
Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our 22,000+ global employees work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™ We continue to earn recognition industrywide, including the 2025 Scrip Award for “Best Contract Research Organization – Full-Service Provider,” 2024 Fierce Biotech CRO Award for "Innovative Approaches to Patient-Centric Research" and the 2024 and 2023 Society for Clinical Research Sites Eagle Award.
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.
Offices: 541 Church at North Hills St, 1000, Raleigh, North Carolina 27609, US
Regulatory and product development consultingearly phase clinical researchphase II-III clinical researchlate phase clinical researcheClinical solutionspatient and site recruitmentmedical device consultingclinical research organizationpharmacovigilancebiotechnology
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