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Associate Director Clinical Research
Job in
Ocala, Marion County, Florida, 34470, USA
Listed on 2025-12-12
Listing for:
Maryland Oncology Hematology
Full Time
position Listed on 2025-12-12
Job specializations:
-
Science
Clinical Research
Job Description & How to Apply Below
Overview
Florida Cancer Affiliates/Ocala Oncology is hiring a full‑time Supervisor Clinical Research for our Ocala office.
Why Work for UsWe offer a competitive benefits package that includes Medical, Dental, Vision, Life Insurance, Short‑term and Long‑term disability coverage, generous PTO, a 401(k) with company match, a Wellness program, Tuition Reimbursement, an Employee Assistance Program, discounts at popular retailers, and more.
Responsibilities- Supervise clinical research staff in accordance with USOR SOP and ICH GCP guidelines.
- Ensure research activities are coordinated with relevant departments and enforce company policies.
- Recruit, interview, hire, assess performance, recommend salary changes, and handle progressive discipline.
- Collaborate with the site research leader (SRL), upper management, and staff to develop accountability standards, metrics, reports, and action plans for quality improvement.
- Participate in study selection, research budget development, and financial objective setting.
- Promote and market the research program within the practice, community, and to referring physicians; coordinate research activities with external sponsors when appropriate.
Starting salary $150K with bonus potential. Visa support may be provided.
- Minimum Master’s degree;
PhD preferred with extensive oncology/clinical drug research experience. - Minimum 5 years of clinical nursing or related scientific discipline experience, preferably oncology; supervisory experience preferred.
- Current licensure as a registered nurse (RN) and current BCLS or ACLS certification;
SoCRA or ARCP certification preferred. - Strong communication, multitasking, and interpersonal skills; ability to thrive in a fast‑paced, constantly changing environment.
- Proficiency in Windows, Excel, and basic computer programs; knowledge of GCP and ICH guidelines, medical terminology, nursing assessment, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, and oncology as related to clinical trials.
- Ability to work in a traditional office environment and to perform required physical tasks (e.g., standing, walking, lifting up to 40 lbs). Reasonable accommodations will be provided where necessary.
Full‑time. Seniority level:
Director.
Position Requirements
10+ Years
work experience
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