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Associate Director Clinical Research

Job in Ocala, Marion County, Florida, 34470, USA
Listing for: Maryland Oncology Hematology
Full Time position
Listed on 2025-12-12
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 150000 USD Yearly USD 150000.00 YEAR
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 Us

We 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.
Qualifications

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.
Employment Type

Full‑time. Seniority level:
Director.

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Position Requirements
10+ Years work experience
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