About this role
Our promise to you:
Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.
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 Background Screening Requirement (Florida Law)
Certain positions are subject to Florida Level 2 background screening, including fingerprinting, as required by state law.
Applicants may review general information about Florida’s background screening requirements at the Florida Care Provider Background Screening Clearinghouse: https://info.flclearinghouse.com/
This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.