5 Academic Center Project Manager I Jobs in Cleveland, OH
OneTen is Hiring an Academic Center Project Manager I Near Cleveland, OH
Job Summary:
THE IDEAL CANDIDATES WILL HAVE A BACKGROUND AS A RNJoin the Cleveland Clinic team, where you will work alongside passionate caregivers and provide patient-first healthcare. Cleveland Clinic is recognized as one of the top hospitals in the nation. At Cleveland Clinic, you will work alongside passionate and dedicated caregivers, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world.
As a Program Manager, you will participate in the project management functions of single and/or multi-institutional research trials, may coordinate/manage day-to-day organization and operational issues and activities related to the performance of Phase I-IV clinical research trials. You will also performs central leadership duties by facilitating key trial communications for academic coordination, providing clinical perspective to the design and conduct of the trial and spearheading initiatives to ensure the quality of study conduct and study performance.
The Future Caregiver is someone who:
• Has High-level management and leadership skills.
• Has written and verbal communication skills.
• Has teamwork and motivational skills.
• Has organizational and multitasking skills.
• Is a RN (Registered Nurse) with clinical experience (Cardiology preferred).
This is a rewarding opportunity that offers growth-oriented projects, mentorship, support, and resources. You will experience great exposure to both the institute and department leadership and have numerous opportunities for career growth in different administrative and project/program management.
At Cleveland Clinic, we know what matters most. That's why we treat our caregivers as if they are our own family, and we are always creating ways to be there for you. Here, you'll find that we offer: resources to learn and grow, a fulfilling career for everyone, and comprehensive benefits that invest in your health, your physical and mental well-being and your future. When you join Cleveland Clinic, you'll be part of a supportive caregiver family that will be united in shared values and purpose to fulfill our promise of being the best place to receive care and the best place to work in healthcare.
Responsibilities:
- Coordinates and contributes to protocol development by understanding of the clinical and regulatory issues related to the diagnosis and treatment of subjects to be studied, current clinical practice and experience with similar protocols.
- Analyzes site strengths and weaknesses as they relate to the intended protocol and selection of qualified investigators/sites.
- Performs ongoing assessment of investigator/site performance.
- Develops or contributes to the performance standards to ensure the integrity of the study, quality of study conduct and study performance.
- Spearheads initiatives to improve quality and makes recommendations to discontinue site if necessary.
- Maintains professional relationships with sponsor, which includes frequent, open communication and associated documentation.
- Prepares and reviews study status reports.
- Acts as a liaison between the Cleveland Clinic sites, sponsors, CRO or other vendors and the FDA.
- Acts as the primary point of contact for the academic leadership committees and coordinates their activity including charter development to ensure successful conduct of the trial.
- Contributes to planned site communication and training (i.e., Investigator meetings, newsletters, study progress updates, telephone communication, supportive reinforcement of sponsor communication, etc.)
- Initiates and develops educational initiatives and tools.
- Maintains knowledge of the Code of Federal Regulations, ICH and GCP guidelines and their application to clinical research sufficient to train others. Other duties as assigned.
Additional Job Duties: Travel will be required for this role
Preferred Qualifications: LPN/RN License
Education:
- Associate's degree in general science or related medical field OR nursing degree/diploma. Bachelor's degree preferred.
Certifications:
- The following certifications are preferred: Certified Clinical Research Professional (CCRP) from the Society of Clinical Research Associates; or Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified Principal Investigator from the Association of Clinical Research Professionals.
Complexity of Work:
- Requires excellent interpersonal, organizational and project management skills.
- Requires demonstrated team leadership, strong communication and problem solving skills.
Work Experience:
- A minimum of five years of clinical research experience. Demonstrated team, leadership, organizational and problem solving abilities.
Physical Requirements:
- Requires full range of motion, manual and finger dexterity and eye-hand coordination.
- Requires normal or corrected hearing and vision to normal range.
- Must be able to sit for long periods of time.
Personal Protective Equipment:
- Follows standard precautions using personal protective equipment.
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Job Summary
Full Time
$83k-106k (estimate)
01/27/2024
06/11/2024
onetengroup.com
<25
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