Veranex is the leading service provider for medtech companies. Our global team of experts help clients anticipate challenges and find solutions throughout the development and commercial lifecycle. Together, we accelerate new technologies to market and improve patient outcomes.
About This Role: Veranex has an exciting opportunity to join our team as a Senior Clinical Data Project Manager. You will be part of a team working to improve lives globally through medical technology innovation. The Senior Clinical Data Project Manager provides a full spectrum of support for clinical data project activities. Responsible for the successful planning, implementation, and execution of contracted services. Manages cross-functional teams and client expectations to achieve client satisfaction.
What You Will Do:
Acts as liaison with client and manages client contractual, organization, and relationship needs/expectations. Ensures clear client communication, process documentation, and compliance with Good Clinical Practices (GCP) and company policies and procedures. Coordinates with functional leads and managers to optimize performance and utilization of project team members. Achieves project quality by identifying quality risks and issues, responding to issues raised by project team members, and planning/implementing appropriate corrective and preventative action plans. Manages scope, schedule, and quality requirements of assigned clinical data project. Fosters strong client relationships at the project level to promote client retention and boost prospective business opportunities. Ensures timely completion of all clinical data project status reporting. Qualifications
Required skills:
Bachelor’s or Master’s degree or international equivalent in Life Sciences Bachelor’s degree or international equivalent and 3-7 years of relevant work experience at a CRO, master’s degree or international equivalent and 2-6 years of relevant work experience at a CRO Strong knowledge of clinical trial life cycle Strong knowledge of regulatory compliance requirements Sound knowledge of clinical data project processes and each function as it relates to biometrics Excellent written and oral communication skills Excellent attention to detail Strong ability to effectively manage multiple tasks and projects Ability to lead and coordinate small teams Preferred: Experience in the medical device industry highly preferred Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.
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About This Role: Veranex has an exciting opportunity to join our team as a Senior Clinical Data Project Manager. You will be part of a team working to improve lives globally through medical technology innovation. The Senior Clinical Data Project Manager provides a full spectrum of support for clinical data project activities. Responsible for the successful planning, implementation, and execution of contracted services. Manages cross-functional teams and client expectations to achieve client satisfaction.
What You Will Do:
Acts as liaison with client and manages client contractual, organization, and relationship needs/expectations. Ensures clear client communication, process documentation, and compliance with Good Clinical Practices (GCP) and company policies and procedures. Coordinates with functional leads and managers to optimize performance and utilization of project team members. Achieves project quality by identifying quality risks and issues, responding to issues raised by project team members, and planning/implementing appropriate corrective and preventative action plans. Manages scope, schedule, and quality requirements of assigned clinical data project. Fosters strong client relationships at the project level to promote client retention and boost prospective business opportunities. Ensures timely completion of all clinical data project status reporting. Qualifications
Required skills:
Bachelor’s or Master’s degree or international equivalent in Life Sciences Bachelor’s degree or international equivalent and 3-7 years of relevant work experience at a CRO, master’s degree or international equivalent and 2-6 years of relevant work experience at a CRO Strong knowledge of clinical trial life cycle Strong knowledge of regulatory compliance requirements Sound knowledge of clinical data project processes and each function as it relates to biometrics Excellent written and oral communication skills Excellent attention to detail Strong ability to effectively manage multiple tasks and projects Ability to lead and coordinate small teams Preferred: Experience in the medical device industry highly preferred Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.
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