Clinical Data Management Specialist

About the job Clinical Data Management Specialist
Principal Duties and Responsibilities:
Collaborate with clients on study design, eCRF design, data review, and data cleaning activities.
Plan, implement, and perform data management tasks and operational aspects of individual projects.
Ensure the quality of data submitted from study sites, assuring timely entry into the database.
Maintain study compliance with the protocol, GCP guidelines, and applicable regulatory requirements.
Track and manage study timelines, project milestones, and potential risks.
Provide support and training to designated staff, contributing to cross-functional tasks and processes.
Foster positive relationships with external vendors and support new system development initiatives.
Communicate with the business development team to manage relationships with external vendors.
Work collaboratively with vendors to develop and implement technical tools supporting business needs.
Support cost proposals, client presentations, and data management at bid defences.
Proactively identify challenges and recommend solutions, supporting vendor and customer audits as assigned.
Qualifications:
A Bachelor's Degree is required.
Strong expertise in GCP and ICH guidelines is essential.
Extensive experience in data review and cleaning is highly desirable.
Computer literacy and proficiency in Microsoft Office with experience in data capture systems is necessary.
Clinical research experience, ideally with a pharmaceutical or medical device company, hospital, or CRO is preferred.
Experience with statistics, programming, and field monitoring is a plus.
Leadership skills and a positive personality are required.
Effective verbal and written communication skills are necessary.
Please apply on the Lifelancer platform at the below link for screening steps & quicker response.