Excell Research is looking for a motivated, experienced professional to serve as a Director of Clinical Research Operations.

Responsibilities

As the Director of Clinical Research Operations, you will be responsible for the direction and management of a team of coordinators and auxiliary staff who conduct pharmaceutical research studies primarily for Central Nervous System and Psychiatric conditions.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Be responsible for clinic operations and oversee the execution of clinical studies in which we perform safety and efficacy tests of pharmaceuticals for the treatment of various CNS and Psychiatric disorders, such as schizophrenia, depression, PTSD, and so forth.
• Ensure quality of execution of studies in line with profitability expectations
• Serve as an escalation point regarding the execution of studies
• Coordinate, as required, with other Excell clinic sites in support of multi-site studies
• Oversee facility operation and maintenance, including preventative maintenance of clinic equipment
• Maintain facility and services through interactions with building mgmt and relevant service providers
• Develop and maintain maintenance schedules for all equipment located in the clinic
• Own supervisory responsibility of both direct and indirect reports (hiring, interviewing, selection, and training of employees along with planning work, performance evaluations, and termination for employees)
• Perform annual performance evaluations on direct reports, and indirect reports, as applicable.
• Review and understand financial reports.
• Interact with client sponsors as needed, working in concert with principal investigators to host sponsors and provide status updates on clinic studies or answers to ad hoc client inquiries
• Support sales and marketing activities related to potential study opportunities
• Adhere to internal standards, policies and procedures.
• Perform other duties as assigned.

Qualifications

Required:

• Bachelor’s degree in a relevant field in science or engineering.
• 2+ years working in a clinic or laboratory with experience following strict safety standards.
• 1+ years supervisory and operational oversight experience.

Preferred:

• Master’s degree in a relevant field in science, engineering, or business.
• 3+ years working in a clinic or laboratory with experience following strict safety standards.
• 2+ years supervisory and operational oversight experience.
• Language Skills: English advanced required.
• Mathematical Skills: intermediate required; experience with statistics preferred.
• Reasoning Skills/Abilities: intermediate required, advanced preferred.
• Computer Skills: advanced proficiency in Microsoft Office Suite preferred, particularly Outlook, Excel, and Word.
• Leadership capabilities.
• Strong verbal and written communication skills.
• Ability to work autonomously.
• Well organized with a strong sense of responsibility for project and time management.
• Ability to handle multiple competing priorities.
• Excellent time management skills are required. Must have a sense of urgency

Job Type: Full-time

Pay: $82,000.00 - $90,000.00 per year

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Retirement plan
• Vision insurance

Schedule:

• 10 hour shift
• 4x10
• Day shift
• No weekends

Ability to commute/relocate:

• Oceanside, CA 92056: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Market research: 1 year (Preferred)
• Project management: 1 year (Preferred)
• Business consulting: 1 year (Preferred)

Work Location: One location

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