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Precision Medicine Associate

Parexel
Parexel
2+ years
Not Disclosed
Hyderabad, India
10 April 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Precision Medicine Associate / Senior Precision Medicine Associate
Location: Hyderabad, Telangana, India
Category: Clinical Trials / Precision Medicine
Employment Type: Full-Time | On-Site
Experience Required: 2+ years in Clinical Trials or Precision Medicine

About the Role
Parexel is seeking a Precision Medicine Associate to support clinical trial execution and operationalize precision medicine strategies within global studies. In this role, you will collaborate closely with Precision Medicine leadership, clinical teams, laboratory personnel, and external vendors to establish standards, manage biomarker analyses, and ensure high-quality and consistent study operations. This role requires hands-on experience with central laboratory management, clinical sample handling, and biomarker-related study activities.

Key Responsibilities

Study Team Collaboration

  • Support cross-functional study teams in clinical trial operations.

  • Manage acquisition, tracking, and handling of clinical trial samples.

  • Provide guidance to clinical study teams regarding sample-related matters.

  • Collaborate with the Informed Consent Form (ICF) Specialist and Precision Medicine Operations Lead (PMOL) to ensure compliance with ICF permissions.

Operational Support for Biomarker & Exploratory Analyses

  • Assist PMOL with selection, oversight, and management of central laboratory and specialty vendors.

  • Execute biomarker plans in collaboration with the study team and PMOL.

  • Contribute to clinical trial documentation under PMOL supervision.

Vendor Management & Coordination

  • Prepare Requests for Proposal (RFPs), review bids, and assess statements of work.

  • Coordinate vendor capability presentations and evaluate central laboratory and specialty vendor performance.

  • Support vendor oversight activities, including audits and academic collaboration communications.

Data Management & Compliance

  • Ensure accurate data acquisition, reconciliation, and information exchange.

  • Provide guidance and training to clinical sites, vendors, and collaborators under PMOL supervision.

  • Comply with Parexel standard operating procedures, ICH-GCP guidelines, and local regulatory requirements.

Qualifications & Experience

  • Bachelor of Science in Biology, Life Sciences, or a related field (Master’s preferred for senior level).

  • Minimum 2 years of relevant industry experience in clinical trials, precision medicine, or translational research.

  • Experience with biomarkers, genomics, proteomics, and cellular assays.

  • Oncology clinical trial experience is highly desirable.

  • Knowledge of bioethics, human biospecimen handling, and research compliance.

Skills & Competencies

  • Strong problem-solving and troubleshooting skills with internal and external stakeholders.

  • Excellent verbal and written English communication skills; local language proficiency preferred.

  • Project management, organizational skills, and ability to prioritize multiple tasks.

  • Proficiency in Microsoft Excel and standard office software; ability to learn role-specific applications.

  • Ability to work effectively in a global matrix environment.

  • Attention to detail, resourcefulness, and ability to maintain data integrity.

Why Join Parexel
This position offers the opportunity to directly impact precision medicine initiatives within clinical trials while working in a global, collaborative environment. You will gain exposure to cutting-edge biomarker and translational research programs, interact with academic collaborators, and contribute to the development of innovative therapies in oncology and other therapeutic areas.

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