Clinical Data Manager Job at Planet Pharma, Los Angeles, CA

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  • Planet Pharma
  • Los Angeles, CA

Job Description

-6 month initial contract, possibility of extension

-Pay: $40.63-43.33/hr

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.

MAIN RESPONSIBILITIES

• 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.

QUALIFICATIONS

Education Level Major/Field of Study

Bachelors Degree Biology, Health Sciences, Mathematics, Computer Science, or equivalent.

Experience/Background

  • Minimum 3 years- 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.

Licenses and Certifications

None required; Certified Clinical Data Manager (CCDM) or equivalent nice to have.

Job Tags

Contract work, Work experience placement,

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