Clinical Data Manager

HireTalent; Los Angeles (CA); On-site; USD 85,000 - 120,000; Full time

Job summary

A healthcare company is seeking a Clinical Data Manager in Sylmar, CA, responsible for managing risk-based quality systems and study data review. The role requires a strong background in clinical operations and project management, aiming to enhance data integrity and safety in trials. Candidates should have a bachelor's degree in life sciences or a related field and at least three years of relevant experience, along with the ability to effectively influence team decisions.

Qualifications

• Minimum 3 years in clinical operations or healthcare-related field.
• Licenses and Certifications: None required; CCDM is a plus.
• Intermediate project management skills with positive team influence.

Responsibilities

• Manage risk-based quality management systems and ensure data completeness.
• Review study data and facilitate stakeholder discussions for impact evaluation.
• Conduct central monitoring activities and direct data cleaning.

Skills

Data Collection Best Practices

Risk Identification

Project Management

Clinical Operations Knowledge

Education

Bachelors Degree in Biology, Health Sciences, Mathematics, or Computer Science

Job description

This position is Non-Exempt.
Will be Onsite located in Sylmar, CA
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
Experience
Experience Details
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.