Top 91 Clinical research coordinator Jobs in Englewood Co

Research Coordinator
Colorado Heart & Vascular, PC —Golden, CO
- $22 - $25 an hour
- Full-time
- Background check
- Management
- Hospital
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
Urology Associates - Denver —Littleton, CO
- Overtime
- Blood sampling
- OSHA
- HIPAA
Quick Apply
Clinical Research Coordinator - Occupational Medicine
National Jewish Health —Denver, CO
- $25.04 - $33.11 an hour
- Full-time
- HIPAA
- Mid-level
- Clinic
- Wellness program
- Health savings account
Clinical Research Coordinator (Melanoma/Derm Team)
University of Colorado —Aurora, CO
- $49,899 - $58,705 a year
- Overtime
- Background check
- Anatomy knowledge
- Vital signs
- Disability insurance
- Health insurance
7d
Program Coordinator, Research Administration
UCHealth —Denver, CO
- $22.80 - $29.64 an hour
- Full-time
- Mid-level
- Office
- Administrative experience
- 403(b) matching
- Health savings account
8d
Clinical Research Professional (Open Rank)
University of Colorado —Aurora, CO
- $48,446 - $72,498 a year
- Overtime
- Hybrid work
- Background check
- Anatomy knowledge
- Surgery
- Disability insurance
- Health insurance
Research Services Clinical Services Professional (Open Rank – Entry and Intermediate Level)
University of Colorado —Aurora, CO
- $49,899 - $72,765 a year
- Overtime
- Hybrid work
- Background check
- Spanish
- Anatomy knowledge
- Disability insurance
- Health insurance
Clinical Research Assistant
CenExel Rocky Mountain Clinical Research —Englewood, CO
- $19 - $22 an hour
- Office
- High school diploma or GED
- Organizational skills
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
ECN Operating LLC —Denver, CO
- $23 - $28 an hour
- 8 hour shift
- Organizational skills
- In-person
- Communication skills
Quick Apply
7d
Open Rank Clinical Research Coordinator (Entry – Senior)
University of Colorado —Aurora, CO
- $49,899 - $78,665 a year
- Overtime
- Background check
- Anatomy knowledge
- Customer service
- Disability insurance
- Health insurance
3d
Clinical Research Coordinator
Quicksilver Scientific, Inc —Louisville, CO
- $72,000 - $88,000 a year
- Full-time
- Hybrid work
- Nursing
- Mid-level
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
3d
Urology Clinical Research Coordinator-RN
AdventHealth Porter —Littleton, CO
- $71,260.80 - $123,215.55 a year
- Full-time
- Spanish
- CPR Certification
- Nursing
- Paid parental leave
- Disability insurance
Oncology Clinical Research Coordinator-RN
AdventHealth Porter —Littleton, CO
- $71,260.80 - $123,215.55 a year
- Full-time
- Spanish
- CPR Certification
- Nursing
- Paid parental leave
- Disability insurance
Clinical Research Point Coordinator – Open Rank Intermediate to Senior
University of Colorado —Aurora, CO
- $52,721 - $72,498 a year
- Overtime
- Hybrid work
- Background check
- Nursing
- Customer service
- Disability insurance
- Health insurance
Lead Clinical Research Coordinator
ECN Operating LLC —Denver, CO
- $30 - $35 an hour
- Weekends as needed
- Mid-level
- Organizational skills
- Leadership
Quick Apply
7d
Clinical Intake Coordinator
GUARDIAN RECOVERY NETWORK HOLDINGS LLC —Denver, CO
- $55,000 - $60,000 a year
- Full-time
- Remote
- LMFT
- Psychiatry
- Addiction Medicine
Quick Apply
2d
Senior Clinical Research Coordinator - Oncology
Children's Hospital Colorado —Aurora, CO
- $25.95 - $38.93 an hour
- Full-time
- Inventory management
- Adults
- 3 years
- Wellness program
- 403(b) matching
Research Services Clinical Sciences Professional OPEN RANK (Entry – Senior) Onsite
University of Colorado —Aurora, CO
- $49,899 - $78,665 a year
- Overtime
- Background check
- Management
- Customer service
- Disability insurance
- Health insurance
3d
Senior Clinical Research Coordinator
Flourish Research —Denver, CO
- $34 - $39 a year
- Nights as needed
- Computer literacy
- Writing skills
- HIPAA
- Paid holidays
- Disability insurance
Quick Apply
Data Coordinator for Clinical Career Advising
Rocky Vista University —Englewood, CO
- $23.25 - $27.50 an hour
- Full-time
- Hybrid work
- Background check
- Microsoft Outlook
- Writing skills
- Paid holidays
- Health insurance

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Research Coordinator

Colorado Heart & Vascular, PC -
Golden, CO

Quick Apply

Job Details

Full-time
$22 - $25 an hour

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Employee discount
Life insurance

Qualifications

Computer operation
Clinical research
HIPAA
Employee relationship building
Driver's License
Bachelor's degree
Document review
Data collection

Full Job Description

Job Title: Research Coordinator 1
Department: Research

Supervisor: Research Manager

GENERAL SUMMARY OF DUTIES:

Responsible for being primary contact on a sub-set of clinical trials; responsibilities include: interacting with patients to complete clinical trial related requirements. Interacting with sponsors to maintain the study in a state of readiness. Primary point of contact for physicians, patients, CHV staff, sponsors, and IRBs to carry out study related protocol and tasks. Responsible for organizing study related material and executing proper practices within study specific protocols.

ESSENTIAL FUNCTIONS:

Understand the principles of clinical research including informed consent, good clinical practice, and human research protection. Able to explain and train junior staff members and non-research staff on these principles so they can participate in clinical research.
Develop strong working relationships and maintain effective communication with study team members, physicians, and study sponsors. Under the direction of the research manager, serve as primary point of contact for sub-set of clinical trials determined by the Research Manager.
Work directly with prospective and enrolled subjects and their families or caregivers, as applicable, including reviewing and completing informed consent, case report forms and other electronic media.
Screen and recruit potential study participants. Work directly with physicians to discuss potential participants and to review inclusion/exclusion criteria.
Review and extract information from electronic medical records and other source documents to complete case report forms and other study related media.
Observe and take notes of hospital-based surgeries and procedures to be able to complete study related material.
Independently, but with oversite from the research manager, will observe trends in clinical research, identify potential areas of growth, and pursue clinical trials in the identified area including, attending conferences to understand scientific fields of interest of physician investigators, identifying and pursing contacts in the research space who may be beneficial to the investigators of CHV, and bringing clinical trials to the research manager and physicians for potential participation.
Without supervision, responsible for overseeing the day-to-day operations of clinical trials and studies.
Must be able to explain complex research protocols at a patient’s level of comprehension. Must be able to patiently explain studies to patient families often times repeatedly.
Able to review legal documents (including CDAs, CTAs, and FUAs) and provide advice to the research manager of changes that are required or items that will not be acceptable. Able to take these documents and create drafts of changes that are acceptable to CHV.
Able to work with a variety of databases to complete manual data entry. Able to oversee and train other research coordinators and act as primary point of contact for junior staff.
Track key study metrics using tracking tools (creating and maintaining documents, tables, databases, spreadsheets, and files), providing timely and quality updates to research manager and/or CHV Leadership.
Under direction of the research manager, must be able to identify the paypoints for a given sub-set of studies, review sponsor provided documentation of payment, identify what procedures, diagnostics or activities remain unpaid and why, and work with sponsor to ensure full payment is received. Create invoices for invoiceable costs and request reimbursement for local IRB oversight/cede.
Adhere to IRB approved protocol for both central and local IRBs. Able to submit documentation to IRBs and address most of the IRB’s questions with and without supervision.
Coordinate protocol related research procedures, study visits, and follow-up care.
Coordinate and lead sponsor, CRO, hospital, physician, or IRB meetings. Must be able to attend or run these meetings. Able to report back to the research manager the content and context of the meeting so that the research manager can act accordingly.
Under supervision of the Research Manager, maintain study source documents and regulatory binders. Report adverse events. Primary contact for sub-set of clinical trials with sponsor monitors are onsite. Able to present study documents in a manner to address all monitor questions in regards to clinical trials.
Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close out activities.
Organize in-person, phone, or online conference meetings with study sponsors and physicians.
Ability to organize and respond to deadlines within the study’s protocol.
Other responsibilities as assigned.

JOB KNOWLEDGE:

Knowledge of CHV’s procedures and systems.
Knowledge of computer systems and applications.
Knowledge of clinical research including GCP, HIPPA, fCOI, etc.
Able to work independently at multiple offices while maintaining strong communication with the rest of the research team.
Utilize appropriate grammar, spelling and punctuation.
Establish and maintain effective working relationships with other employees and the public.
Communicate and present information effectively.
Identify problems and work to find appropriate solutions.
Ability to prioritize tasks and be flexible with changes in schedules.
Ability to read, understand and follow oral and written instructions.
Must have valid driver’s license and auto insurance.

SKILLS:

Possesses interpersonal skills necessary to interact with people.
Ability to coordinate with various parties participating within a study.
Ability to navigate various electronic data capture systems.
Ability to navigate electronic medical records systems
Data Entry.

PHYSICAL / MENTAL REQUIREMENTS:

Work may require collecting data within a fast-paced hospital setting; requires manual dexterity sufficient to operate a keyboard, calculator, telephone, copier, and fax machine. Vision must be correctable to 20/20 and hearing must be in normal range for telephone contacts.

TYPICAL WORKING CONDITIONS:

Work is performed in a fast-paced office environment and within the hospital. Involves frequent contact with physicians, clinical staff, hospital staff, study sponsors, and patients. Work may be stressful at times.

TEAMWORK:

The success of CHV is based upon every member working together to help the team accomplish its goal. Teamwork requires cooperation and a group effort. When CHV’s goals are achieved, the individual team members will also benefit. Research relies on working with and supporting the efforts of clinicians and other office professionals, research coordinators are expected to exemplify teamwork.

EDUCATION:

Bachelor’s degree; familiarity with MS office, excel, and an understanding of cardiology.

EXPERIENCE REQUIRED:

Clinical (particularly cardiovascular) experience required. One to two years experience as clinical research coordinator. Experience as mentor or trainer preferred. Demonstrate strong leadership and problem-solving abilities with high level interpersonal skills. Possess a strong work ethic.

Job Type: Full-time

Pay: $22.00 - $25.00 per hour

Benefits:

401(k)
Dental insurance
Employee discount
Health insurance
Life insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

clinical research coordinator jobs in englewood co

Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator - Occupational Medicine

Clinical Research Coordinator (Melanoma/Derm Team)

Program Coordinator, Research Administration

Clinical Research Professional (Open Rank)

Research Services Clinical Services Professional (Open Rank – Entry and Intermediate Level)

Clinical Research Assistant

Clinical Research Coordinator

Open Rank Clinical Research Coordinator (Entry – Senior)

Clinical Research Coordinator

Urology Clinical Research Coordinator-RN

Oncology Clinical Research Coordinator-RN

Clinical Research Point Coordinator – Open Rank Intermediate to Senior

Lead Clinical Research Coordinator

Clinical Intake Coordinator

Senior Clinical Research Coordinator - Oncology

Research Services Clinical Sciences Professional OPEN RANK (Entry – Senior) Onsite

Senior Clinical Research Coordinator

Data Coordinator for Clinical Career Advising

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