Columbia University
Clinical Research Coordinator I - CBCH
Columbia University, Independence, Kansas, United States, 67301
Job Type: Officer of Administration
Regular/Temporary: Regular
Hours Per Week: 35
Salary Range: $66,300 - $80,000 Annual
The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting.
Position Summary We are an innovative research center looking for highly organized, detail-oriented, andenthusiastic candidates to support the patient-oriented research portfolio of the Center.Under the direction of the Principal Investigator, the Clinical Research Coordinator I will assist
with participant recruitment, onboarding, scheduling, and data collection for research studies. This position offers a unique opportunity to advance participant care while contributing tocutting-edge research on innovative cardiac rehabilitation (CR) models. The candidate canexpect to represent the Center by interacting with a wide variety of multi-disciplinary personnelat our Center, including study PIs, research coordinators, data team personnel andadministration, as well as external clinic representatives and key collaborators. The candidatemust be able to demonstrate flexibility in workload and work hours to meet critical deadlines.Further, we anticipate developing new studies and research directions, so ideal candidates willbe able to adapt to a fast-paced environment with evolving responsibilities, workloads and workschedules.
At CBCH our goal is to work together as a collective (faculty, admin, and staff) to advance sharedvalues and goals.
Candidates should anticipate the need to work both on site (in the research office and in clinicalspaces), as well as remotely. Candidates should anticipate the need for flexible work hours toattain study goals and grant milestones. Candidates may expect work hours to be scheduledbetween 7:00 am and 7:30 pm and occasionally on weekends, varying from week-to-weekdepending upon study and grant needs. Candidates should be comfortable in a team-oriented,collaborative work culture with frequent interactions with studyparticipants, collaborating investigators, and clinic personnel.
Responsibilities
Assist with participant recruitment, eligibility screening, and scheduling.
Conduct home-based CR sessions via telehealth, including safety checks, RPMintegration, exercise supervision, and maintain appropriate documentation of patientcare in Epic/MyChart.
Lead participant onboarding sessions, providing training on devices, exerciseequipment, vital sign measurements, apps, RPE scale, and safety protocols.
Recognize contraindications and abnormal participant responses to exercise.
Respond appropriately to all situations, including exercise cessation and referral tomedical professionals.
Collect and manage study-related data including session adherence, vital signs, andpatient-reported measures.
Collaborate with the study team to identify and report significant observations.
Ensure fidelity to study protocol while integrating with standard-of-care CR workflows.
Perform other duties as assigned.
Minimum Qualifications
Master’s degree in Clinical Exercise Physiology or related field plus 600 hours ofclinical experience or equivalent in education, training and experience.
Strong communication and participant education skills.
Proficiency in exercise testing, ECG interpretation, and risk stratification.
Current CPR/BLS (Professional Rescuer) certification (or obtained prior to start date).
Preferred Qualifications
ACSM Clinical Exercise Physiologist (CEP) or AACVPR Certified Cardiac Rehabilitation Professional (CCRP) credential.
Advanced experience with Epic/MyChart and telehealth delivery platforms.
Prior experience in cardiac rehabilitation or secondary prevention.
Research experience, including participant recruitment and data collection.
Other Requirements
Strong interpersonal skills, as well as oral and written communication skills, including arecord of work in research settings (e.g., presentations/publications).
Experienced in participant-oriented, clinical research.
Must be highly organized, with excellent attention to detail and follow-up skills.
High technical competence related to the use of research devices.
Must be able to work independently, as well as perform as part of a team.
Must demonstrate flexibility and willingness to adjust schedule to meet project demandsand critical deadlines, including availability for early morning, late evening or potentiallyweekend hours.
Strong commitment to equity, diversity, and inclusion.
Participation in medical surveillance program:
Contact with patients and/or human research subjects
Must successfully complete applicable compliance and systems training requirements.
Equal Opportunity Employer / Disability / Veteran Columbia University is committed to the hiring of qualified local residents.
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Regular/Temporary: Regular
Hours Per Week: 35
Salary Range: $66,300 - $80,000 Annual
The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting.
Position Summary We are an innovative research center looking for highly organized, detail-oriented, andenthusiastic candidates to support the patient-oriented research portfolio of the Center.Under the direction of the Principal Investigator, the Clinical Research Coordinator I will assist
with participant recruitment, onboarding, scheduling, and data collection for research studies. This position offers a unique opportunity to advance participant care while contributing tocutting-edge research on innovative cardiac rehabilitation (CR) models. The candidate canexpect to represent the Center by interacting with a wide variety of multi-disciplinary personnelat our Center, including study PIs, research coordinators, data team personnel andadministration, as well as external clinic representatives and key collaborators. The candidatemust be able to demonstrate flexibility in workload and work hours to meet critical deadlines.Further, we anticipate developing new studies and research directions, so ideal candidates willbe able to adapt to a fast-paced environment with evolving responsibilities, workloads and workschedules.
At CBCH our goal is to work together as a collective (faculty, admin, and staff) to advance sharedvalues and goals.
Candidates should anticipate the need to work both on site (in the research office and in clinicalspaces), as well as remotely. Candidates should anticipate the need for flexible work hours toattain study goals and grant milestones. Candidates may expect work hours to be scheduledbetween 7:00 am and 7:30 pm and occasionally on weekends, varying from week-to-weekdepending upon study and grant needs. Candidates should be comfortable in a team-oriented,collaborative work culture with frequent interactions with studyparticipants, collaborating investigators, and clinic personnel.
Responsibilities
Assist with participant recruitment, eligibility screening, and scheduling.
Conduct home-based CR sessions via telehealth, including safety checks, RPMintegration, exercise supervision, and maintain appropriate documentation of patientcare in Epic/MyChart.
Lead participant onboarding sessions, providing training on devices, exerciseequipment, vital sign measurements, apps, RPE scale, and safety protocols.
Recognize contraindications and abnormal participant responses to exercise.
Respond appropriately to all situations, including exercise cessation and referral tomedical professionals.
Collect and manage study-related data including session adherence, vital signs, andpatient-reported measures.
Collaborate with the study team to identify and report significant observations.
Ensure fidelity to study protocol while integrating with standard-of-care CR workflows.
Perform other duties as assigned.
Minimum Qualifications
Master’s degree in Clinical Exercise Physiology or related field plus 600 hours ofclinical experience or equivalent in education, training and experience.
Strong communication and participant education skills.
Proficiency in exercise testing, ECG interpretation, and risk stratification.
Current CPR/BLS (Professional Rescuer) certification (or obtained prior to start date).
Preferred Qualifications
ACSM Clinical Exercise Physiologist (CEP) or AACVPR Certified Cardiac Rehabilitation Professional (CCRP) credential.
Advanced experience with Epic/MyChart and telehealth delivery platforms.
Prior experience in cardiac rehabilitation or secondary prevention.
Research experience, including participant recruitment and data collection.
Other Requirements
Strong interpersonal skills, as well as oral and written communication skills, including arecord of work in research settings (e.g., presentations/publications).
Experienced in participant-oriented, clinical research.
Must be highly organized, with excellent attention to detail and follow-up skills.
High technical competence related to the use of research devices.
Must be able to work independently, as well as perform as part of a team.
Must demonstrate flexibility and willingness to adjust schedule to meet project demandsand critical deadlines, including availability for early morning, late evening or potentiallyweekend hours.
Strong commitment to equity, diversity, and inclusion.
Participation in medical surveillance program:
Contact with patients and/or human research subjects
Must successfully complete applicable compliance and systems training requirements.
Equal Opportunity Employer / Disability / Veteran Columbia University is committed to the hiring of qualified local residents.
#J-18808-Ljbffr