Clinical Research Coordinator jobs in Boulder, CO
Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Recently Added Clinical Research Coordinator jobs
Clinical Research Coordinator/RN
- The US Oncology Network
-
BOULDER, CO
OTHER
-
Overview:
Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator (RN) in Boulder.
We realize that it sounds cliché but it is true - taking care of cancer patients is a calling. It's much more than a job. Each of us has a unique story that brought us to Rocky Mountain Cancer Centers (RMCC), but those stories usually share common themes of care, compassion, and commitment.
No matter the role each RMCC team member serves in, the goal is the same: to provide the best care possible for each and every one of our patients. Whether we are a nurse holding our patient's hand, or a scheduler on the phone finding an appointment that fits into a patient's schedule, we are deeply connected to our patients and do what we can to help.
If this sounds like you, we'd love to have you join our team.
Salary Range: $60,000-$75,000 for non-nurses and $80,000-$95,000 for nurses
Pay is based on several factors including but not limited to education, work experience, certification, etc.
A wide salary range is posted for this position and any job offer is based upon a salary analysis to comply with the Colorado Equal Pay for Equal Work Act. The salary analysis considers relevant experience, education, and certifications as compared to others doing substantially similar work. While all offers are compliant with the Colorado Equal Pay for Equal Work Act, there is no guarantee an offer will be at the top of the posted range based on the salary analysis.
As of the date of this posting, in addition to your salary, RMCC offers the following benefits for this position, subject to eligibility requirements: Health, dental, and vision plans; wellness program; health savings account; flexible spending accounts; potential for research bonus depending on financials of department after one year of employment; 401(k) retirement plan; life insurance, short-term disability insurance; long-term disability insurance, Employee Assistance Program; PTO, holiday pay, tuition reimbursement, and employee paid critical illness and accident insurance.
We will be accepting applications on an ongoing basis for this position. To apply for this position, start the process by clicking the blue "apply" button.
Responsibilities:
Job Profile Summary
Responsible for recruiting, screening, consenting, and enrolling patient in clinical trials. CRC II also coordinates and oversees the subject's visits in accordance with the protocol requirements. Duties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers. Acts as resource for the education and training of clinic staff as well as resource for problem solving of complex issues for the implementation of the research process throughout the clinic, process improvements and SOPs. Compiles and reports protocol activity; accrual data, and financial information. Assures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA. Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards.
Key Responsibilities- Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials.
- Coordinates patient care in compliance with protocol requirements. May disburse investigational drug. Maintains investigational drug accountability. Oversees the preparation of orders by physicians to assure that protocol compliance is maintained. Packages and ships lab specimens to central vendors where applicable. Required to complete Hazmat and/or IATA training.
- In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings and participates in data collection of all subjects.
- Responsible for preparing study-related documentation such as protocol worksheets, adverse event reports, institutional review board documents, and annual continuing review reports.
- Maintains regulatory documents in accordance with USOR SOP and applicable regulations. May participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite. May collaborate with Research Site Leader in the study selection process.
- Participates in required training and education programs. May be responsible for education of clinic staff regarding clinical research. Collaborates with staff in the development of action plans and performance improvement opportunities with staff to improve quality.
- May be responsible for compiling and reporting protocol activity, accrual trends, data entry compliance, and research financial information to practice administration and physicians. May be responsible for reviewing protocol specific billing guides and submitting billing information to appropriate personnel.
CRC II- Minimum Job Qualifications (Knowledge, Skills, & Abilities)
Education/Training -- Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
- Minimum three years of experience in a clinical or scientific related discipline required, preferably in oncology.
- SoCRA or ACRP certification preferred.
RN II- CRC
Minimum Job Qualifications (Knowledge, Skills, & Abilities):
Education/Training -- Graduate from an accredited program for nursing education required (BSN preferred)
- SoCRA or ACRP certification preferred.
- Current licensure as a registered nurse in state of practice
- Current BLCS or ACLS certification required.
- OCN certification strongly preferred.
Business Experience -- Minimum 3 years of nursing experience required, preferably in oncology.
- Experience in clinical research preferred.
Additional Experience -- Experience in Microsoft Office
- Experience working with physicians preferred.
- Experience working in clinical research is preferred.
Specialized Knowledge/Skills -- Must have excellent communication skills.
- Excellent organizational skills
- Strong ability to multi-task
- Excellent time management skills
- Must have strong interpersonal skills to be able to interact with multiple people on many different levels.
- Must have a high level of attention to detail.
- Must be able to work in a fast-paced environment.
- May be responsible for basic clinical assessments.
Working Conditions:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations will be offered to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an
oncology/hematology clinic environment.
Physical Requirements (Lifting, standing, etc.) -- Large percent of time performing computer-based work is required
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations will be offered to enable individuals with disabilities to perform the essential functions. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.
All qualified candidates are required to pass a background check and non-federal drug test (which excludes marijuana) post offer of employment and prior to hire.
Candidates will be required to show proof of being vaccinated against influenza upon commencing employment. Reasonable accommodations will be considered on a case-by-case basis for exemptions to this requirement in accordance with applicable law. - 20 Days Ago
Clinical Research Specialist
- Medtronic
-
Boulder, CO
FULL_TIME
- Clinical Lab Clinical Research Specialist (Clinical Research) In this exciting role as a Clinical Research Specialist, you will have primary responsibility to manage day-to-day operations of clinical ...
- 2 Days Ago
Clinical Research Specialist
- Medtronic
-
Boulder, CO
FULL_TIME
- Clinical Lab Clinical Research Specialist (Clinical Research) In this exciting role as a Clinical Research Specialist, you will have primary responsibility to manage day-to-day operations of clinical ...
- 2 Days Ago
Dental Office Insurance and Treatment Coordinator
- Grand Junction Dental Office Patient Coordinator...
-
Grand Junction, CO
FULL_TIME
- Come join our beautiful new location and the same amazing team. Our private practice is looking for an amazing full-time dental insurance and treatment coordinator to join our team. We are an establis...
- 12 Days Ago
Research Associate
- Steadman Philippon Research Institute
-
Vail, CO
FULL_TIME
- DescriptionThe Steadman Philippon Research Institute (SPRI) is known throughout the world for our research into the causes, prevention, and treatment of orthopaedic disorders. We are committed to solv...
- 12 Days Ago
Clinical Training Coordinator
- COLORADO WEST INC
-
Grand Junction, CO
OTHER
- Job Details Job Location: Psych Hospital - Grand Junction, CO Position Type: Full Time Salary Range: $32.22 Hourly DescriptionMedical, Dental, Vision, PTO Accrual, and 403b Benefits Available. Positio...
- 22 Days Ago
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0 Clinical Research Coordinator jobs found in Boulder, CO area
Clinical Research Coordinator - Critical Care
- Careerbuilder
-
Denver, CO
- Clinical Research Coordinator - Critical Care Facility *National Jewish Health - Main Campus Department Clinical Researc...
- 4/29/2024 12:00:00 AM
Clinical Nurse Coordinator
- Hiring Now!
-
Englewood, CO
- Description Hourly Wage Estimate: $43.13 - $61.67 / hour Learn more about the benefits offered for this job. The estimat...
- 4/29/2024 12:00:00 AM
Clinical Nurse Coordinator Labor and Delivery
- Hca
-
Denver, CO
- Hourly Wage Estimate: $36.98 - $55.48 / hourLearn more about the benefits offered for this job.The estimate displayed re...
- 4/29/2024 12:00:00 AM
Clinical Nurse Coordinator
- Hiring Now!
-
Denver, CO
- Description Hourly Wage Estimate: $39.68 - $56.74 / hour Learn more about the benefits offered for this job. The estimat...
- 4/28/2024 12:00:00 AM
Clinical Nurse Coordinator NICU
- Hiring Now!
-
Aurora, CO
- Description Hourly Wage Estimate: $43.13 - $61.67 / hour Learn more about the benefits offered for this job. The estimat...
- 4/28/2024 12:00:00 AM
Clinical Nurse Coordinator Med Surg
- North Suburban Medical Center
-
Denver, CO
- Description Hourly Wage Estimate: $36.98 - $55.48 / hour Learn more about the benefits offered for this job. The estimat...
- 4/28/2024 12:00:00 AM
Clinical Nurse Coordinator RN Neuroscience
- Hiring Now!
-
Aurora, CO
- Description Hourly Wage Estimate: $36.98 - $55.48 / hour Learn more about the benefits offered for this job. The estimat...
- 4/28/2024 12:00:00 AM
Operating Room Clinical Nurse Coordinator
- Synergy Surgery Center
-
Englewood, CO
- Description Hourly Wage Estimate: $42.72 - $64.08 / hour Learn more about the benefits offered for this job. The estimat...
- 4/27/2024 12:00:00 AM
About Boulder, Colorado
Boulder (/ˈboʊldər/) is the home rule municipality that is the county seat and the most populous municipality of Boulder County, Colorado, United States. It is the state's 11th most populous municipality; Boulder is located at the base of the foothills of the Rocky Mountains at an elevation of 5,430 feet (1,655 m) above sea level. The city is 25 miles (40 km) northwest of Denver.
The population of the City of Boulder was 97,385 people at the 2010 U.S. Census, while the population of the Boulder, CO Metropolitan Statistical Area was 294,567. Boulder is known for its association with American fr...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$63,165 to $85,169
Boulder, Colorado area prices
were up 2.3% from a year ago
were up 2.3% from a year ago
What does a Clinical Research Coordinator do?
Clinical Research Coordinator in Monterey, CA
Coordinators often become the front line for patients because they feel more comfortable with us.
November 07, 2019
Clinical Research Coordinator in Bakersfield, CA
If you have a medical experience you may need a certificate program to work as a CRC bt if there is none then you will need an education program that covers all the required medical and research coursework in clinical research.
October 27, 2019
Clinical Research Coordinator in New Bedford, MA
If you’re looking for a job you can complete at home that lets you use your organizational and leadership skills, a career in clinical research coordination could be for you.
October 09, 2019