The right talent can transform your business—and we make that happen. At Collabera, we go beyond staffing to deliver strategic workforce solutions that drive growth, innovation, and agility. With deep industry expertise, a global talent network, and a people-first approach, we connect you with professionals who don’t just fit the role but elevate your business. Partner with us and build a workforce that powers success.
Clinical Data Manager - 100 Per Cent Onsite
Contract: Sylmar, California, US
Salary Range: 40.00 - 48.00 | Per Hour
Job Code: 362684
End Date: 2025-07-06
Days Left: 16 days, 13 hours left
Position Details:
Industry: Medical Devices/Nutraceuticals
Job Title: Clinical Data Manager - 100% Onsite
Location: Sylmar, CA 91342
Duration: 09+ months [+ Possibilities of extension]
Pay Range: $40-$48/hr
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.
-
This position for a Clinical Data Manager will oversee 3-5 clinical trials from data management perspective, and together with assigned Coordinator, takes care of all related activities from CRF design, clinical data review and oversight, to trial closure related data activities.
Job 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:
-
Bachelor’s degree-Major/Field of Study- Biology, Health Sciences, Mathematics, Computer Science, or equivalent
-
3 years in clinical operations or healthcare related field.
-
Knowledge of data collection best practices for clinical trials.
-
Knowledge of global clinical operations.
-
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.
-
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.
Job Requirement
- Clinical Data Manager
- Clinical Data Management
- Project Management
- Clinical Operations
- CDISC
- ADaM
- STDM
- CRF
- Medidata
Reach Out to a Recruiter
- Recruiter
- Phone
- Niharika Shrivastava
- niharika.shrivastava@collabera.com
Apply Now
Apply Now
