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Full-Time Opportunity: This is a permanent, full-time position with a competitive package and real career growth potential.
Job Description
Required Qualifications
- 10+ years of experience in Clinical Data Management , including roles as CDM, Sr. CDM, and/or Project Manager.
- Proven experience in eClinical and eCOA implementation across global clinical trials.
- Strong command of EDC systems such as Medidata Rave , Oracle InForm , and Veeva Vault .
- Familiarity with data standards (CDISC, SDTM), medical coding (MedDRA, WHO Drug), and regulatory compliance .
- Demonstrated ability to lead studies independently , manage complex timelines, and coordinate with integral stakeholders.
- Experience in specialty data functions such as pharmacovigilance, IRT, and lab data oversight.
- Excellent communication, leadership, and problem-solving skills .
- PMP certification is highly desirable.
Key Responsibilities
- Lead end-to-end implementat...