For those who want to keep growing, learning, and evolving. We at Kelly® hear you, and we’re here for you! We’re seeking an Associate Director to work at a biopharmaceutical company that discovers, develops, and commercializes innovative therapeutics in areas of unmet medical need in Santa Monica, CA. Sound good? Take a closer look below. You owe it to yourself to consider this great new opportunity. Pay Rate: $107 (depending on the experience) per hour Why you should apply to be an Associate Di... more details
For those who want to keep growing, learning, and evolving. We at Kelly® hear you, and we’re here for you! We’re seeking an Associate Director to work at a biopharmaceutical company that discovers, develops, and commercializes innovative therapeutics in areas of unmet medical need in Santa Monica, CA. Sound good? Take a closer look below. You owe it to yourself to consider this great new opportunity.
Pay Rate: $107+ (depending on the experience) per hour
Why you should apply to be an Associate Director:
Competitive pay rate with potential for a temp-to-hire position.
Opportunity to work with a reputable biopharmaceutical company.
Convenient morning shift schedule.
Onsite position offering stability and growth opportunities.
What’s a typical day as an Associate Director? You’ll be:
Drive the development, optimization, alignment, and implementation of clinical trial processes.
Partner with equivalent functions at Gilead for shared clinical trial processes.
Identify and lead process improvement opportunities.
Establish and maintain training curricula for Clinical Operations and other Clinical Development functions.
Develop onboarding plans for Clinical Operations.
Support transition planning within Clinical Operations.
Monitor compliance with procedural documents and training requirements.
Develop and report process and training compliance metrics.
Participate in internal audits and regulatory inspections.
Support audit/inspection response development and CAPA implementation.
Stay updated on industry and regulatory changes.
Promote compliance awareness and culture.
This job might be an outstanding fit if you: Must-Haves:
In-depth knowledge of international GCP regulatory requirements.
Understanding of end-to-end clinical trial processes.
Ability to independently lead and manage cross-functional initiatives.
Excellent communication skills.
Ability to negotiate sensitive issues objectively.
Critical and creative thinking for problem-solving.
Ability to prioritize and adjust workload.
Leadership by example to promote quality and compliance.
Nice-to-Haves:
Experience with clinical operations procedural documents.
Familiarity with clinical trial process optimization.
Experience with developing training curricula and onboarding plans.
Experience with compliance metrics and reporting.
Experience with internal audits and regulatory inspections.
Knowledge of ICH E6 (R3) guidelines.
What happens next Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all our recruiters will have access to your profile, expanding your opportunities even more.
Helping you discover what’s next in your career is what we’re all about, so let’s get to work. Apply to be an Associate Director today!
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