Associate Clinical Data Manager
Posted:
Company Details
Name:IQVIA
Industry:
Hospital & Health Care
Website:
https://www.iqvia.com/
Description:
IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical …
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Job Details
Job Type:
Full Time
Workplace Type:
On-site
Qualification:
Diploma
Job Experience:
Mandatory
Job Location:
Nairobi County, Kenya
Closing Date:
Undisclosed
Salary:
Undisclosed
Other Pay:
Benefits
Job Category:
Telecommunications
Job Description
Job Overview
- We are seeking an experienced and detail-oriented Associate Lead Data Manager to oversee data management activities across multiple clinical projects. In this role, you will ensure high-quality data delivery in line with sponsor requirements, while collaborating with cross-functional teams, sites, and external partners.
Key Responsibilities
- Gather study set-up requirements through effective communication with stakeholders.
- Lead database set-up, configuration, and validation to ensure optimal study design and data integrity.
- Support validation and implementation of new device integrations.
- Perform ongoing data cleaning activities to ensure accurate, timely, and high-quality deliverables.
- Ensure all outputs meet established quality standards and client expectations.
- Train and mentor new team members.
- Lead internal study meetings, participate in sponsor meetings, and support audits and study kick-offs.
- Track and manage project progress, identify risks, and implement corrective actions in collaboration with the Data Team Lead (DTL).
- Oversee database revisions and support the adoption of new technologies.
- Collaborate with programming teams to drive process improvements and automation initiatives.
- Ensure compliance with all required training and electronic SOPs (eSOPs).
- Contribute expertise to the development, review, and maintenance of standard operating procedures (SOPs) and work instructions.
- Maintain effective, collaborative communication with leadership, line managers, and cross-functional teams.
Qualifications & Requirements
- Education: Master’s degree in Life Sciences / Postgraduate in Science / Bachelor of Pharmacy or equivalent preferred.
- Strong understanding of the drug development lifecycle and overall clinical research processes.
- Proficiency in English (spoken and written).
- Advanced skills in Microsoft Office applications (Excel, Word, Outlook).
- Strong analytical, organizational, and problem-solving abilities.
- Excellent communication and stakeholder management skills.
- Ability to manage multiple projects and meet deadlines in a fast-paced environment.
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