Parexel

Clinical Data Analyst II

Parexel  •  Hyderabad, IN (Onsite)  •  3 hours ago
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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.

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.
  • Experience in Oncology, Hematology, Cardiovascular, Fibrosis, and/or Cell Therapy studies preferred.
  • CCDM Certification is advantageous.
  • Stable employment history with tenure of at least one year with previous employers or a valid explanation for transitions.

Qualification

Bachelor's Degree in Life Sciences, Pharmacy, Clinical Research, Biotechnology, or a related field.

Parexel

About Parexel

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 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.

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Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Raleigh, North Carolina
Year Founded
Unknown
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