jobs in OPIS

全职 Clinical Data Manager 工作, 薪水, OPIS Melaka 公司招聘中 - Ricebowl

Clinical Data Manager

Undisclosed

Malacca City, Melaka

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工作地点

  • Jalan Kota Malacca City Melaka Malaysia

职位描述

岗位职责

As a Senior Clinical Data Manager, you’ll work closely with Sponsors and cross-functional teams to oversee database development, data cleaning, quality control, and database lock activities, while supporting process improvements and mentoring junior team members.

What You'll Do:
  • Lead clinical data management activities in compliance with CDISC standards, regulatory requirements, and OPIS SOPs.
  • Design, validate, and maintain eCRFs, clinical databases, and related data management documentation.
  • Perform data cleaning, coding activities, SAE reconciliation, quality checks, and database lock activities.
  • Act as the main point of contact for Sponsors and study teams on data management matters.
  • Track study milestones, manage project deliverables, and proactively identify and escalate risks.
  • Support audits, inspections, process improvements, and the development of data management standards.
  • Mentor junior team members and contribute to study-specific training activities.
What You Bring:
  • Bachelor's degree in a scientific or related discipline.
  • At least 7 years of clinical data management experience within a CRO, biotech, pharmaceutical company, or research organisation.
  • Strong knowledge of CDISC standards, ICH-GCP, ISO14155, FDA 21 CFR Part 11, and clinical data management processes.
  • Experience with clinical databases, eCRF systems, and data management tools.
  • Excellent communication skills in English and the ability to work effectively in international teams.
  • Strong organisational skills, attention to detail, and a quality-focused mindset.
What We Offer:
We offer a competitive salary, additional benefits, and the opportunity to grow your career within a collaborative and expanding international organisation.

Who We Are:
Founded in 1998 in Italy, OPIS is a full-service, science-driven CRO providing clinical trial management, biometrics, regulatory, pharmacovigilance, and medical writing services worldwide. Our experienced teams support clients through every stage of clinical development, delivering high-quality solutions across a broad range of therapeutic areas.
 

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