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Clinical Research Coordinator

Quick overview

The coordinator screens patients for protocol eligibility, manages the informed consent process, and coordinates patient care in compliance with research protocols. They are also responsible for accurate data collection, regulatory documentation, and collaborating with physicians to monitor adverse events.

Requirements summary

Requires an associate's degree with 5 years of clinical experience or a nursing degree with 3 years of experience, preferably in oncology. Necessary certifications include BLS or ACLS, with SoCRA or ACRP certifications preferred.

associate degreebachelor degreeprofessional certificateCommunication SkillsPatient MonitoringProblem SolvingMedical TerminologyPatient EducationDatabase ManagementData CollectionRegulatory DocumentationOncology NursingInformed ConsentClinical AssessmentPatient ScreeningProtocol ComplianceClinical Trial CoordinationDrug AccountabilityGCP Concepts

Job description

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 at our Skyridge location.
Bring your established Oncology and or Research experience and join a team dedicated to providing an excellent experience to patients.
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-$97,000 for nurses Pay is based on several factors including but not limited to education, work experience, certification, etc. 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. 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.

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 protocol. Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide patient teaching regarding administration. Maintains investigational drug accountability.

Benefits

Accident Insurance
Critical Illness Insurance
Dental Insurance
Employee Assistance Program
Life Insurance
Wellness Program
Paid Time Off
Holiday Pay
Health Insurance
Vision Insurance
Health Savings Account
Tuition Reimbursement
Flexible Spending Accounts
401(k) Retirement Plan
Long-term Disability Insurance
Short-term Disability Insurance
Research Bonus

Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.Minimum five years of experience in a clinical or scientific related discipline required, preferably in oncology.
SoCRA or ACRP certification preferred. or Graduate from an accredited program for nursing education (BSN preferred).
Minimum seven years of nursing experience, preferably in oncology.
Experience in clinical research preferred.
Current licensure as a registered nurse in state of practice.
Current BLCS or ACLS certification required.
OCN, SoCRA or ACRP certification preferred.
Specialized Knowledge/Skills - Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents.
Ability to work independently, organize, prioritize, and follow through with results Ability to solve practical problems and implement solutions Strong ability multi-task Must have excellent communication skills Excellent time management skills Must have a 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 Attention to details and accuracy Knowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medical, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, clinical trials and GCP concepts Experience with computer data entry and database management 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 may be made 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 may be made 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. (This description is general in nature and is not intended to be an exhaustive list of all responsibilities.
Other duties may be assigned as needed to meet company goals.) 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.
This job posting will remain open until we have identified an adequate applicant pool.
Applicants are strongly encouraged to apply early.
To apply for this position, start the process by clicking the blue "apply" button.

Clinical Research Coordinator

Quick overview

Requirements summary

Job description

Overview

Salary Range

Responsibilities

Benefits

Qualifications

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