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...