
Manager, Clinical Data Management
Posted 1 day ago

Posted 1 day ago
This is a fully remote position, open to applicants in United States.
• Lead the clinical data management team.
• Manage project management documentation.
• Execute clinical data management activities and system implementations for EDETEK’s CONFORM eClinical.
• Develop design specifications for system forms, reports, and associated components.
• Facilitate the testing of system implementations.
• Supervise data management projects to guarantee quality, timely delivery, and continuous client satisfaction.
• Identify client requirements and create innovative project solutions utilizing expertise, operational capabilities, and technology.
• Engage in communication with clients and internal teams.
• Support internal initiatives in clinical data management.
• Complete traditional and assigned data management operations and tasks.
• Communicate client requirements and issues, enforce standard operating procedures, and monitor project progress and timelines.
• Assist in developing and maintaining systems that support project infrastructure.
• Collaborate with Clinical Data Specialists to implement Data Management Plans.
• Lead communication with clients and sponsors to provide contracted clinical data management services with high quality and integrity.
• Ensure the proper filing of required documentation according to EDETEK and project standards.
• Oversee User Acceptance Testing for new software.
• Select and interview candidates for clinical data manager positions.
• Train and mentor junior team members.
• Proficient in effective communication in English, both in person and through phone and written correspondence.
• Ability to lead functional meetings.
• Exceptional attention to detail and accuracy is essential.
• Strong organizational skills.
• Proven ability to manage multiple projects simultaneously.
• Capability to work collaboratively, effectively, and productively in diverse organizational structures.
• Ability to work independently, take initiative, and meet deadlines: Delivering Excellence, Serving Customers, Accountability and Ownership, Global and Cross-Functional Communication.
• Experience in a team-oriented, collaborative setting.
• Adaptability to thrive in a continuously changing environment.
• Skill in prioritizing and executing tasks effectively in a high-pressure environment.
• Advanced computer skills with practical knowledge of MS Office and potentially project management software.
• A Bachelor’s degree or an equivalent combination of education, training, and experience is mandatory. A degree in a scientific, medical, or technological field is preferred.
• At least 2 years of experience in clinical trials or clinical data management, or related industry experience/training is required.
• Previous responsibility for the entire data management life-cycle is preferable.
• Working knowledge of EDC studies and SAS is necessary.
• Corporate office environment.
• Some travel (5%) may be required, with potential for weekend travel.
• Cross-functional interactions.
• Choice of comprehensive Medical, Vision, and Dental Insurance plans.
• Paid vacation time and sick leave.
• Annual corporate holidays.
• Participation in the 401K Plan.
• Extensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, and more.
• Health Advocate and Employee Assistance Program.
ICON plc
ICON plc
MSD
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