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At K2 Medical Research, a privately-owned clinical research facility in the greater Orlando and Central Florida area, we specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. We are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research and connecting our patients with the treatments of tomorrow, we can improve the health of our local communities, and by extent, the population of our world.
K2 is seeking an experienced
Lead Project Manager / Clinical Research Coordinator
to lead a team of clinical research professionals at our
Tampa
clinic. The Lead Project Manager assists the Director with the day-to-day operations and provides leadership, training, and support to the clinical staff to ensure high quality, ample volume, and efficient productivity. They maintain effective and positive working relationships with subjects, sponsors, Investigators, and employees.
Primary Responsibilities:
Train new and current Project Managers and Research Assistants to ensure effective coordination in the clinical trials processes
Assist Project Managers and Research Assistants with assigned tasks as necessary
Ensure pre-screens convert to screens and screens convert to randomizations
Monitor team’s workload, schedule, and capacity
Provide clinical support and assistance in the assignment of PM’s, Raters, and other staff
Troubleshoot and resolve clinic, protocol, and SOP issues
Assist with assigned tasks as necessary
Problem solves protocol issues
Work closely with the Director to improve and streamline clinic processes
Work with Director, Recruitment, and other clinical team managers as necessary to find ways to increase visit volume
Liaison between PM team and other departments to ensure smooth, effective, and quality workflow
Assist the Director with projects and tasks as assigned
Acting Supervisor or point of contact in the absence of the Director Maintains quality service and departmental standards by reading, understanding, and adhering to organizational Standard Operating Procedures (“SOP”)
Assist in establishing and enforcing departmental standards with study protocol adherence as necessary
Explore new opportunities to add value to organization and departmental processes
Support the organization’s mission and goals
Attend applicable company-sponsored training
Assist with PM team staffing planning, interviews, and performance evaluations
Responsible for maintaining PM team PTO and schedule coverage
Knowledge, Skills, and Abilities:
Outstanding verbal and written communication skills
Excellent interpersonal and customer services skills
Strong time management and organizational skills In depth knowledge of industry regulations
Proven ability to and foster mentoring relationships
Ability to create momentum and foster organizational change
Qualifications:
Bachelor’s degree in a health-related field
3 years of Clinical Research experience
Strong working knowledge of GCP and FDA guidelines
Knowledge of medical terminology
BLS Healthcare Provider required
Applicants that do not meet 100% of the above qualifications but who have a combination of related education and applicable experience may be considered upon approval
Benefits:
At K2, we value our employees and their professional and personal needs, and support these through our benefit offerings:
Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term and Life Insurance, Short Term , Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs.
401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested
PTO of 16 days per year, 17 days after the first year of FT employment
9 paid Holidays
K2 observes a four-day work week, Monday through Thursday, for full time employees. Fridays are non-working days unless required by business needs.
Join the K2 Family: Where Compassion and Connection Lead the Way!
At K2 Med, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff. We thrive on empathy, a patient-first approach, and absolutely
zero big egos
(unless it's an ego about being extra kind, then we'll allow it!). We believe a supportive, caring experience is paramount for our patients, and that starts with you.
We celebrate what makes you uniquely you! Your , , , marital status, , , or even your favorite snack (though we're partial to good research snacks) don't define your talent or fit here. If you need a little extra support or accommodation due to a , no sweat! Just reach out to our friendly team at HR@k2med.com, and we'll ensure you have everything you need to shine.
At K2 Medical Research, a privately-owned clinical research facility in the greater Orlando and Central Florida area, we specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. We are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research and connecting our patients with the treatments of tomorrow, we can improve the health of our local communities, and by extent, the population of our world.
K2 is seeking an experienced
Lead Project Manager / Clinical Research Coordinator
to lead a team of clinical research professionals at our
Tampa
clinic. The Lead Project Manager assists the Director with the day-to-day operations and provides leadership, training, and support to the clinical staff to ensure high quality, ample volume, and efficient productivity. They maintain effective and positive working relationships with subjects, sponsors, Investigators, and employees.
Primary Responsibilities:
Train new and current Project Managers and Research Assistants to ensure effective coordination in the clinical trials processes
Assist Project Managers and Research Assistants with assigned tasks as necessary
Ensure pre-screens convert to screens and screens convert to randomizations
Monitor team’s workload, schedule, and capacity
Provide clinical support and assistance in the assignment of PM’s, Raters, and other staff
Troubleshoot and resolve clinic, protocol, and SOP issues
Assist with assigned tasks as necessary
Problem solves protocol issues
Work closely with the Director to improve and streamline clinic processes
Work with Director, Recruitment, and other clinical team managers as necessary to find ways to increase visit volume
Liaison between PM team and other departments to ensure smooth, effective, and quality workflow
Assist the Director with projects and tasks as assigned
Acting Supervisor or point of contact in the absence of the Director Maintains quality service and departmental standards by reading, understanding, and adhering to organizational Standard Operating Procedures (“SOP”)
Assist in establishing and enforcing departmental standards with study protocol adherence as necessary
Explore new opportunities to add value to organization and departmental processes
Support the organization’s mission and goals
Attend applicable company-sponsored training
Assist with PM team staffing planning, interviews, and performance evaluations
Responsible for maintaining PM team PTO and schedule coverage
Knowledge, Skills, and Abilities:
Outstanding verbal and written communication skills
Excellent interpersonal and customer services skills
Strong time management and organizational skills In depth knowledge of industry regulations
Proven ability to and foster mentoring relationships
Ability to create momentum and foster organizational change
Qualifications:
Bachelor’s degree in a health-related field
3 years of Clinical Research experience
Strong working knowledge of GCP and FDA guidelines
Knowledge of medical terminology
BLS Healthcare Provider required
Applicants that do not meet 100% of the above qualifications but who have a combination of related education and applicable experience may be considered upon approval
Benefits:
At K2, we value our employees and their professional and personal needs, and support these through our benefit offerings:
Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term and Life Insurance, Short Term , Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs.
401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested
PTO of 16 days per year, 17 days after the first year of FT employment
9 paid Holidays
K2 observes a four-day work week, Monday through Thursday, for full time employees. Fridays are non-working days unless required by business needs.
Join the K2 Family: Where Compassion and Connection Lead the Way!
At K2 Med, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff. We thrive on empathy, a patient-first approach, and absolutely
zero big egos
(unless it's an ego about being extra kind, then we'll allow it!). We believe a supportive, caring experience is paramount for our patients, and that starts with you.
We celebrate what makes you uniquely you! Your , , , marital status, , , or even your favorite snack (though we're partial to good research snacks) don't define your talent or fit here. If you need a little extra support or accommodation due to a , no sweat! Just reach out to our friendly team at HR@k2med.com, and we'll ensure you have everything you need to shine.