All the benefits and perks you need for you and your family: - Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance
- Paid Time Off from Day One
- 403-B Retirement Plan
- 4 Weeks 100% Paid Parental Leave
- Career Development
- Whole Person Well-being Resources
- Mental Health Resources and Support
- Pet Benefits
Schedule: Full time
Shift: Day (United States of America)
Address: 301 E PRINCETON ST
City: ORLANDO
State: Florida
Postal Code: 32804
Job Description: - Leads the development and submission of investigator-initiated research protocols, contributing to study design, scientific rationale, and regulatory documentation.
- Reports to the Scientific Director, Senior or Associate Investigator, or designated program lead, and performs other duties as assigned to support research success and professional development.
- Supports protocol-specific research activities, including laboratory, clinical, or data-focused tasks, in collaboration with multidisciplinary teams.
- Engages in scientific writing and supports the preparation of grant applications in coordination with internal teams and external collaborators.
- Collaborates with research staff, core teams, and investigators to coordinate study activities and ensure protocol adherence.
- Participates in committee meetings, academic discussions, and collaborative planning efforts as assigned by program leadership.
- Ensures compliance with all institutional, local, state, and federal policies and regulations governing the conduct of research and human subjects protections.
- Fulfills Institutional Review Board (IRB) and NIH training and compliance requirements, and maintains up-to-date documentation for all assigned studies.
- Reviews study-related documents, including protocols, consent forms, and investigator brochures, ensuring alignment with regulatory and institutional standards.
- Generates research funding from industry, federal, and non-federal sources to support research efforts, with a goal of meeting annual revenue targets as defined by the research institute ($250,000).
- Mentors post-doctoral fellows, graduate students, or junior staff by providing guidance in research tasks, data collection, and scientific development.
- Contributes to manuscript writing, abstract preparation, and the development of presentations that communicate research findings.
- Other duties as assigned.
Knowledge, Skills, and Abilities: • Established competency in research and the regulatory environment as evidenced by published research and peer-reviewed work [Required]
• Knowledge of all regulatory requirements that pertain to clinical/medical research [Required]
• Knowledge or experience in Calorimetry or Multi-Nuclear Spectroscopy [Preferred] [Required]
Education: • Doctorate [Required]
Field of Study: • Biomedical science field including, but not limited to, Biology, Chemistry, Exercise Science, Physiology, Pharmacodynamics
• Proven history of National Institutes for Health (NIH) and/or Pharmaceutical research in the areas of diabetes, metabolism, and the metabolic origins of cardiovascular disease Required
• Experience in an academic/teaching environment where career development of staff was evidenced Required
Work Experience: • 1+ experience in the clinical/translational research environment [Required]
• Experience in an academic/teaching environment where career development of staff was evidenced [Required]
Additional Information: • An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement
• Proven history of National Institutes for Health (NIH) and/or Pharmaceutical research in the areas of diabetes, metabolism, and the metabolic origins of cardiovascular disease [Required]
Licenses and Certifications: • N/A
Physical Requirements: (Please click the link below to view work requirements)
Physical Requirements - https://tinyurl.com/msy4mja2
Pay Range:$80,204.80 - $149,177.60