Clinical Site Leader With Top-Tier AMRC Site Network at BioPharma Select | Torre

Clinical Site Leader With Top-Tier AMRC Site Network

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Full-time

Legal agreement: Employment

Base compensation
USD150k - 180k/year

+ Bonuses (up to 10% of base compensation)

Negotiable
location_on
Bellflower, CA, USA
Posted 6 months ago

Responsibilities


Clinical Site Leader Role: N. Irvine, CA. About the Site Network: - Top-tier AMRC Clinical Site Network. - This research site specializes in early phase clinical trials. - Specialty areas of research include psychiatry, acute post-op pain, and neurology. - Each site has extensive experience and expertise in complex early phase trials. - All sites have in-patient capability. Benefits: - Highly competitive compensation and a generous benefits package to full-time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Job Summary: - Responsible for overseeing the day-to-day administrative and operational functions of the business and improvement of business procedures. Compensation: - $150-180K per year, depending on education, experience, and skillset. Essential Responsibilities and Duties: - Implements practices to ensure compliance with operational policies, objectives, and initiatives. - Executes HR activities with recruitment, interview coordination, employee onboarding, and training to ensure smooth business operations. - Develops budget and ensures financial and operational metrics are meeting organizational objectives by identifying, analyzing, and monitoring issues that affect profitability, growth, and productivity. - Executes business strategy in an efficient and financially responsible manner to attain short- and long-term goals. - Reports directly to the COO. - Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all-inclusive. Education/Experience/Skills: - Early phase non-academic clinical research site management. - Psychiatric/CNS trial experience. - Bachelor's Degree is preferred. - 5 years’ experience in clinical research. - Experience managing clinical research staff. - Working knowledge of Microsoft Office Suite, including PowerBI and Teams, preferred. Working Conditions: - Indoor, Office environment. - Essential physical requirements include sitting, typing, standing, and walking. - Lightly active position, occasional lifting of up to 20 pounds. - Reporting to work, as scheduled, is essential. Equal Opportunity Employer: - Our client is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.