Clinical Data Manager (W2 only)

We have Contract role Clinical Data Manager (W2 Only) for our client at Maple Grove MN. Please let me know if you or any of your friends would be interested in this position.

Position Details: Clinical Data Manager (W2 Only) - Maple Grove MN Location : Maple Grove MN 55311 Project Duration : This is a 6-month contract with potential to extend highly likely Hours : 9:00am-5:00 PM May potentially become a Hybrid role after 3-4 months training, but will be 100 % onsite to start with Onsite/Remote : Could possibly be Hybrid role- will be decided once training is completed and manager has had the opportunity to observe the candidate s work performance

Job Description

The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk-based quality management systems, as described in the risk assessment, data management plan, and site and central monitoring plans.

As the customer-face of Data Review and its primary liaison with the therapy group, the Clinical Data Manager's therapy-specific knowledge ensures alignment to customer definitions of criticality, and informs review and analysis of study data.

Identification of study specific risks to study conduct and human subject safety; analysis of risks; development and implementation of mitigation strategies.
Review of study data to detect anticipated and unanticipated issues related to trial data completeness and quality.
Facilitate multi-stakeholder discussions to review findings, evaluate impact and develop action plans for correction and continued monitoring.
Conduct Central Monitoring activities, as described in Central Monitoring Plan.
Direct all data cleaning activity related to assigned studies.

Experience:

• 3 years in clinical operations or healthcare related field.
• Education and work experience in project management, life sciences and/or technical field.
• Knowledge of data collection best practices for clinical trials.
• Knowledge of global clinical operations.
• Experience in consultative role, with Subject Matter Expertise, and effectively influencing a team decision to the desired outcome.
• Proficient at the identification of risks in a process, evaluation of likelihood and impact, and the development of effective mitigation and monitoring strategies that are imperfect yet meet the business need.
• Proficient in the translation of clinical trial requirements to the technical specifications required for effective data collection.
• Skilled at making inferences and connections based on limited information, clearly describing the knowns, unknowns, and alternative explanations.
• Intermediate project management skills; developing a multifaceted plan with complex dependencies and holding peers accountable to adherence to the plan while maintaining positive and collaborative relationships.
• Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.