Neuroscience Program Mgr

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:

6061

S Willow Dr City:

Greenwood Village State:

Colorado Postal Code:

80111

Job Description:

Manages the administrative and scientific implementation of research protocols for complex and/or multiple research studies. Develops and monitors research protocols, ensuring compliance with regulatory requirements and institutional policies. Oversees the preparation, submission, and management of grant applications, including NIH grants. Coordinates and conducts training sessions on grant application procedures and research protocols. Provides guidance on protocols, regulations, and guidelines to principal investigators and research staff. Collaborates with faculty, trainees, and personnel in drafting and editing scientific content for grants, contracts, manuscripts, and research protocols. Ensures accurate and timely reporting of grant activities, milestones, and deliverables. Maintains ongoing updates and communications related to current grants and contracts. Manages budgetary aspects of grants and contracts, ensuring proper allocation and use of funds. Supervises and supports research staff involved in grant and contract management. Serves as a liaison with internal departments and external entities, including funding agencies and collaborators. Participates in executive and steering committees for large-scale, multi-site studies.

Knowledge, Skills, and Abilities:

• Excellent interpersonal skills and the ability to effectively communicate with all levels of personnel- executives, management, staff, Physician Investigators and supporting teams - Self-motivated and detail-orientated, with good organizational, follow-up, computer and analytical skills. [Required]
• Able to establish priorities and problem-solve. [Required]
• A deep understanding and experience with the clinical trial process and operations, from execution through completion. [Required]
• Demonstrate experience aggregating study and sponsor and/or funder-related information for comprehensive scientific, operational and administrative review in a timely manner. [Required]
• Ability to conduct oneself professionally, maintaining confidence, confidentiality, integrity and objectivity. [Required]
• Ability to work well with others, using tact and diplomacy in verbal and written communications, while demonstrating teamwork skills. [Required]
• Proficient in Microsoft Office (Outlook, Word, Excel, PowerPoint), and other relevant computer programs. [Required]
• Flexible and comfortable working in a fast-paced environment [Required]
• Proven communication skills - oral, written, presentation, formal and informal [Required]
• Interpersonal skills and the ability to communicate with all levels of employees (Executive, [Required]
• Management and staff) both written and verbally [Required]
• Self-motivated and detail-oriented, with good organizational, follow-up, computer, and analytical skills [Required]
• Excels in a constantly changing environment with competing priorities [Required]
• Ability to prioritize projects assigned and ability to operate well under pressure and heavy workloads to meet deadlines. [Required]
• Acts as a role model; inspires teams to go beyond their role expectations to help each other and exceed project goals. [Required]
• Ability to conduct oneself professionally, maintaining confidence, confidentiality, integrity, and objectivity. [Required]
• Two years related experience [Preferred]
• Knowledge of the key principles of clinical trials design and practice.

[Preferred]

Education:

• Bachelor's [Required]

Field of Study:

N/A Work Experience:

• 5+ experience managing of projects and/or programs [Required]

Additional Information:

N/A Licenses and Certifications:

• Certified Associate in Project Management (CAPM) [Preferred]
• Project Management Professional (PMP) [Preferred]
• Association of Clinical Research Professionals (ACRP) [Preferred]

Physical Requirements:

(Please click the link below to view work requirements) Physical Requirements - https://tinyurl.com/msy4mja2

Pay Range:

$74,422.15 - $153,539.38 This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.