Clinical Device Management Analyst — Trials Support
Planet Pharma
Irvine (CA)
On-site
USD 34,440 - 48,216
Full time
14 days+
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Job summary
A healthcare solutions firm based in California is seeking a Clinical Device Management Associate Analyst to support device processes for clinical trials. This role involves managing inventory, ensuring compliance with regulations, and providing training on device accountability. Candidates should have a Bachelor's degree and at least 1 year of clinical trial experience. Strong problem-solving, organizational, and communication skills are essential. This position offers a salary of $25-35/hr and requires on-site work five days a week.
Qualifications
Minimum 1 year of clinical trial support or Clinical operations experience required.
Experience with ERP software and CTMS preferred.
Must have strong written and verbal communication skills.
Responsibilities
Manage inventory and device accountability for clinical sites.
Ensure compliance with regulatory guidelines and internal procedures.
Compile and analyze data to support regulatory submissions.
Skills
Strong problem-solving skills
Organizational skills
Analytical skills
Attention to detail
Communication skills
Interpersonal relationship skills
Education
Bachelor's Degree in related field
Tools
Salesforce
JD Edwards (ERP software)
MS Office Suite
Job description
A healthcare solutions firm based in California is seeking a Clinical Device Management Associate Analyst to support device processes for clinical trials. This role involves managing inventory, ensuring compliance with regulations, and providing training on device accountability. Candidates should have a Bachelor's degree and at least 1 year of clinical trial experience. Strong problem-solving, organizational, and communication skills are essential. This position offers a salary of $25-35/hr and requires on-site work five days a week.