Clinical Research Coordinator I
Rocky Mountain Cancer Centers
Date: 2 days ago
City: Boulder, Colorado
Contract type: Full time
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 in Boulder.
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 cliche 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.
Hourly range for CRC I Applicants: $25.00-$29.00
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.
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.
Assists with patient care in compliance with protocol requirements. May
disburse investigational drug and maintain investigational drug
accountability. Participates in data collection, entry, and reporting for
the subjects.
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.
Participates in required training and education programs as well as monitoring
and auditing activities. May work directly with sponsors. May participate in
scheduling monitoring and auditing visits, as well as interact with the
monitors/auditors while onsite.
Assists with collection and maintenance of regulatory documents in accordance
with USOR SOPs and applicable regulations.
May assist in the packing and shipping of lab specimens to central vendors.
May be required to complete Hazmat and/or IATA training.
Qualifications
Associate's degree in a clinical or scientific related discipline
Required, Bachelor's Degree Preferred.
One year of experience in a clinical or scientific related discipline,
Preferably In Oncology Preferred. Previous Clinical Research Experience
required.
Business Experience -
Experience in Microsoft Office
Experience Working With Physicians 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-aced 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 accommodati ns 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.
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.
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.
The US Oncology Network is an Equal Opportunity Employer. All qualified
applicants will receive consideration for employment without regard to race,
color, religion, sex, national origin, sexual orientation, gender
identity, disability or protected veteran status.
Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive
provider of cancer care has an exciting opportunity for an experienced
Clinical Research Coordinator in Boulder.
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 cliche 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.
Hourly range for CRC I Applicants: $25.00-$29.00
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.
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.
Assists with patient care in compliance with protocol requirements. May
disburse investigational drug and maintain investigational drug
accountability. Participates in data collection, entry, and reporting for
the subjects.
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.
Participates in required training and education programs as well as monitoring
and auditing activities. May work directly with sponsors. May participate in
scheduling monitoring and auditing visits, as well as interact with the
monitors/auditors while onsite.
Assists with collection and maintenance of regulatory documents in accordance
with USOR SOPs and applicable regulations.
May assist in the packing and shipping of lab specimens to central vendors.
May be required to complete Hazmat and/or IATA training.
Qualifications
Associate's degree in a clinical or scientific related discipline
Required, Bachelor's Degree Preferred.
One year of experience in a clinical or scientific related discipline,
Preferably In Oncology Preferred. Previous Clinical Research Experience
required.
Business Experience -
Experience in Microsoft Office
Experience Working With Physicians 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-aced 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 accommodati ns 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.
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.
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.
The US Oncology Network is an Equal Opportunity Employer. All qualified
applicants will receive consideration for employment without regard to race,
color, religion, sex, national origin, sexual orientation, gender
identity, disability or protected veteran status.
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