Data Management Specialist - London, ON NB L
4 weeks ago

KGK Science is a world-leading Contract Research Organization specializing in the conduct of human research studies and regulatory services for the Natural Health Product industry.
Responsibilities
- Develops and reviews data management SOPs and updates as needed.
- Develops the data management plan (DMP) and updates as required
Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
Clinical Trial Recruitment Team Lead
1 week ago
The Clinical Trial Recruitment Team Lead plays a key operational role in supporting participant recruitment for clinical trials and acts as the primary support to the Recruitment Manager. This position is responsible for executing recruitment strategies, coordinating recruitment ...
Clinical Trial Study Start-up Coordinator
1 week ago
The Clinical Trial Start-Up Coordinator is responsible for end-to-end start-up and IRB/REB activities for clinical trials conducted by the Clinical Research Organization (CRO). This role owns the preparation, submission, tracking, and maintenance of IRB/REB applications and appro ...
Human Research Study Start-up Coordinator
1 week ago
The Human Research Study Start-Up Coordinator is responsible for end-to-end start-up and IRB/REB activities for human research studies. This role owns the preparation, submission, tracking, and maintenance of IRB/REB applications and approvals. · Draft and customize informed cons ...