Job Description
Job Description
Description :
The Associate Director of Clinical Trials is responsible for overseeing the strategic and operational aspects of clinical trials. This role involves managing trial execution, ensuring compliance with regulatory requirements, and driving the development and implementation of clinical trial strategies. The Associate Director will work closely with cross-functional teams, including research, regulatory affairs, finance, and external partners, to ensure the successful completion of clinical trials and advancement of clinical research objectives.
Strategic Planning and Management :
Regulatory Compliance :
Team Leadership and Coordination :
Study Design and Implementation :
Budget and Resource Management :
Data Management and Analysis :
Stakeholder Engagement :
Problem Solving and Troubleshooting :
Reporting and Documentation :
Admin duties as assigned by manager
Requirements : Education / Training
Licenses / Certifications
CITI Program Training in Good Clinical Practice (GCP) required
CITI Program Training in Human Subjects Protection (HSP) required
Experience Requirements
Minimum of 5-10 years of experience in clinical research, with a focus on clinical trial management, coordination, or regulatory compliance.
Proven track record in leading and managing clinical trials across multiple phases (I-IV) in various therapeutic areas, required.
At least 3-5 years of supervisory or management experience within a clinical research setting, including mentoring and leading a team of clinical research professionals.
Experience with regulatory submissions, including IRB protocols, informed consent forms, and clinical trial agreements.
Demonstrated expertise in developing and implementing standard operating procedures (SOPs) to ensure compliance with FDA regulations and ICH-GCP guidelines.
Experience in managing clinical trial budgets, contracts, and site negotiations is preferred.
Strong network within the clinical research community and established relationships with key industry stakeholders is an advantage.
Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The work of this position is performed in an environmentally controlled medical practice environment. The position requires the ability to work under pressure and with a diverse population, including staff, physicians, clients, patients, insurance companies and other members of the public on a regular basis. The position may cause frequent exposure to communicable diseases, bodily fluids, toxic substances, ionizing radiation, medicinal preparations and other conditions common to a clinical environment.
This position may require occasional travel to study sites and external meetings.
Work is typically performed in an office setting with potential for remote work flexibility.
Compensation Package
At BASS Medical Group, we understand that a comprehensive, high quality, and affordable health benefits program is now more essential than ever. The overall well-being of our employees is at the forefront of our focus. With this in mind, we offer our eligible employees a generous benefits program.
Health & Welfare Benefits : Medical through Anthem Blue Cross PPO, Low-Cost Dental and Vision, Medical FSA & HSA.
Retirement Savings & Income Security : Basic Life & AD&D Insurance, Long Term Disability, 401K plan with an employer contribution, Access to Financial Advisors, Identity Theft Program.
Work / Life Balance Benefits : Paid Time Off and Company Paid holidays, Life Assistance Program, Commuter & Parking Benefits, Secure Travel Services, Healthy Rewards Program, Will Preparation Program, Additional perks to include discounts for Cellular phone and Gym memberships.
Voluntary Benefits : Optional Life & AD&D Insurance, Aflac Supplemental Insurance, Pet Insurance
Compensation will be based on experience
Pay Scale / Ranges : $125,000.00 / year
Clinical Trial Associate • Walnut Creek, CA, US