$26 - $34.50/hr
... in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the ... Experience in a medical, scientific research, or technology-oriented business environment is also ...
$26 - $34.50/hr
... in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the ... Experience in a medical, scientific research, or technology-oriented business environment is also ...
... in a professional research environment. Key Responsibilities: Serve as PI or Sub-I on assigned clinical trials. Conduct medical screenings, physical examinations, and participant assessments. Ensure ...
... in a professional research environment. Key Responsibilities: Serve as PI or Sub-I on assigned clinical trials. Conduct medical screenings, physical examinations, and participant assessments. Ensure ...
Physician Allergy/Immunology - Competitive Salary
$190K - $230K/yr
Medical
Dental
Vision
Retirement
PTO
Opportunity to participate in clinical trials and research programs* Involvement in fellowship training program in partnership with academic medical campus--- Clinical & Academic Details:* Provide ...
Physician Allergy/Immunology - Competitive Salary
$190K - $230K/yr
Medical
Dental
Vision
Retirement
PTO
Opportunity to participate in clinical trials and research programs* Involvement in fellowship training program in partnership with academic medical campus--- Clinical & Academic Details:* Provide ...
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
Research Services Senior Professional / Senior Clinical Sciences Professional
Aurora, CO · On-site
Medical
Dental
Vision
Life
Retirement
PTO
Knowledge of basic human anatomy, physiology, medical terminology * Advanced knowledge of GCP, FDA Rules and Regulations in relation to clinical trials, NIH guidelines, ICH guidelines and HIPAA ...
Research Services Senior Professional / Senior Clinical Sciences Professional
Aurora, CO · On-site
Medical
Dental
Vision
Life
Retirement
PTO
Knowledge of basic human anatomy, physiology, medical terminology * Advanced knowledge of GCP, FDA Rules and Regulations in relation to clinical trials, NIH guidelines, ICH guidelines and HIPAA ...
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
... IV clinical trials in Denver, CO. This role involves overseeing protocol compliance, ensuring ... Conduct medical screenings, physical exams, and assessments of study participants. * Provide ...
... IV clinical trials in Denver, CO. This role involves overseeing protocol compliance, ensuring ... Conduct medical screenings, physical exams, and assessments of study participants. * Provide ...
... IV clinical trials in Denver, CO. This role involves overseeing protocol compliance, ensuring ... Conduct medical screenings, physical exams, and assessments of study participants. * Provide ...
... IV clinical trials in Denver, CO. This role involves overseeing protocol compliance, ensuring ... Conduct medical screenings, physical exams, and assessments of study participants. * Provide ...
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
S. medical license (CO and/or IL preferred). * Board certification in Dermatology or one of the ... Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
Clinical Study Monitor-Animal Health
Fort Collins, CO · Remote
$33.25 - $45.25/hr
Primary Job Purpose Responsible for performing monitoring activities to ensure clinical trials are conducted in compliance with study protocols, VICH GL9 GCP guidelines, and applicable regulatory ...
Clinical Study Monitor-Animal Health
Fort Collins, CO · Remote
$33.25 - $45.25/hr
Primary Job Purpose Responsible for performing monitoring activities to ensure clinical trials are conducted in compliance with study protocols, VICH GL9 GCP guidelines, and applicable regulatory ...
Clinical Study Monitor-Animal Health
Fort Collins, CO · On-site
$68K - $120K/yr
Primary Job Purpose Responsible for performing monitoring activities to ensure clinical trials are conducted in compliance with study protocols, VICH GL9 GCP guidelines, and applicable regulatory ...
Clinical Study Monitor-Animal Health
Fort Collins, CO · On-site
$68K - $120K/yr
Primary Job Purpose Responsible for performing monitoring activities to ensure clinical trials are conducted in compliance with study protocols, VICH GL9 GCP guidelines, and applicable regulatory ...
Senior Clinical Research Coordinator
Denver, CO · On-site
$34 - $39/hr
Medical
Dental
Vision
Life
Retirement
PTO
In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of ... medical ethics, IRB, GCP and ICH guidelines. * Complete all required training in a timely manner.
Senior Clinical Research Coordinator
Denver, CO · On-site
$34 - $39/hr
Medical
Dental
Vision
Life
Retirement
PTO
In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of ... medical ethics, IRB, GCP and ICH guidelines. * Complete all required training in a timely manner.
Senior Clinical Research Coordinator
Denver, CO · On-site
$34 - $39/hr
Medical
Dental
Vision
Life
Retirement
PTO
In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of ... medical ethics, IRB, GCP and ICH guidelines. * Complete all required training in a timely manner.
Quick apply
Senior Clinical Research Coordinator
Denver, CO · On-site
$34 - $39/hr
Medical
Dental
Vision
Life
Retirement
PTO
In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of ... medical ethics, IRB, GCP and ICH guidelines. * Complete all required training in a timely manner.
Senior Clinical Research Coordinator
$34 - $39/hr
Medical
Dental
Vision
Life
Retirement
PTO
In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of ... medical ethics, IRB, GCP and ICH guidelines. * Complete all required training in a timely manner.
Senior Clinical Research Coordinator
$34 - $39/hr
Medical
Dental
Vision
Life
Retirement
PTO
In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of ... medical ethics, IRB, GCP and ICH guidelines. * Complete all required training in a timely manner.
Principal Investigator/Clinical Research Rheumatologist position in Denver, CO - Part Time (0-8hr)
$100 - $250/hr
... clinical trials. * Conduct medical screenings, physical examinations, and specialty-specific ... Participate in site initiation visits, monitoring visits, audits, and investigator meetings.
Principal Investigator/Clinical Research Rheumatologist position in Denver, CO - Part Time (0-8hr)
$100 - $250/hr
... clinical trials. * Conduct medical screenings, physical examinations, and specialty-specific ... Participate in site initiation visits, monitoring visits, audits, and investigator meetings.
As a Medical Assistant you will perform medical assistant related procedures for patients enrolled in clinical trials. * You will access, flush and de-access ports. * You will perform peripheral and ...
As a Medical Assistant you will perform medical assistant related procedures for patients enrolled in clinical trials. * You will access, flush and de-access ports. * You will perform peripheral and ...
As a Medical Assistant you will perform medical assistant related procedures for patients enrolled in clinical trials. * You will access, flush and de-access ports. * You will perform peripheral and ...
As a Medical Assistant you will perform medical assistant related procedures for patients enrolled in clinical trials. * You will access, flush and de-access ports. * You will perform peripheral and ...
As a Medical Assistant you will perform medical assistant related procedures for patients enrolled in clinical trials. * You will access, flush and de-access ports. * You will perform peripheral and ...
As a Medical Assistant you will perform medical assistant related procedures for patients enrolled in clinical trials. * You will access, flush and de-access ports. * You will perform peripheral and ...
Medical In Clinical Trials information
What is the difference between Medical In Clinical Trials vs Clinical Research Coordinator?
| Aspect | Medical In Clinical Trials | Clinical Research Coordinator |
|---|---|---|
| Credentials | Medical degree or relevant healthcare certification | Bachelor's degree, often in health or science fields |
| Work Environment | Hospitals, clinics, research centers | Research sites, hospitals, clinics |
| Employer & Industry | Pharmaceutical companies, CROs, academic institutions | Research organizations, hospitals, clinics |
| Primary Focus | Overseeing patient care and medical procedures in trials | Managing study logistics, data collection, and compliance |
Medical In Clinical Trials typically involves direct patient care and medical oversight during clinical studies, requiring healthcare credentials. In contrast, Clinical Research Coordinators focus on managing study operations and data. Both roles are essential in clinical research but differ in responsibilities and qualifications.
What are popular job titles related to Medical In Clinical Trials jobs in Colorado?
For Medical In Clinical Trials jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Medical In Clinical Trials jobs in Colorado look for?
The top searched job categories for Medical In Clinical Trials jobs in Colorado are:
What cities in Colorado are hiring for Medical In Clinical Trials jobs?
Cities in Colorado with the most Medical In Clinical Trials job openings:
$26 - $34.50/hr
Full-time
Re-posted 3 days ago
Dana-Farber Cancer Institute rating
8.1
Based on 20 frontline employees who took The Breakroom Quiz
Job description
The Clinical Research Coordinator will work within the Brighton Dana-Farber Satellite clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI disease programs. The Satellite CRC will be responsible for the primary data collection, management of patient clinical information, and regulatory documents as it pertains to participation in clinical trials across all studies open at the Satellite site(s). Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains site regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for site IRB submissions (violations, deviations, severe adverse event reports). This individual may also screen patients for protocol eligibility, obtain informed consent (minimal risk studies), and register study participants to clinical trials. Travel to the Longwood campus and other DFCI Satellite sites may be required. This position is based at the Brighton campus.
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.
KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:
MINIMUM JOB QUALIFICATIONS:
The position requires a bachelor's degree, with 0 to 1 year of related experience preferred. Experience in a medical, scientific research, or technology-oriented business environment is also preferred. The role requires close to moderate supervision.
SUPERVISORY RESPONSIBILITIES: None
PATIENT CONTACT: Minimal patient contact.
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
EEO Poster
Pay Transparency Statement
The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate's relevant experience, skills and qualifications.
For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).
$48,100.00 - $54,400.00
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.
- Oversight of the clinical trials regulatory process at the DFCI Satellite(s) and site activation activities
- Communication and coordination with the lead study team at the Longwood campus for study start-up, ongoing study team meetings, and project management of all site study activities
- Responsible for data reporting and management, collection of source documents, use of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries for all studies at the Satellite site(s)
- Prepare and/or complete regulatory related reports and IRB submissions as it pertains to the satellite's studies. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis
- Maintains various regulatory tracking databases with information related to study recruitment, subject enrollment, and study progress and completion
- Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations
- Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
- Coordination and management of all clinical trials at the Satellite site(s), including communication with Sponsors and regulatory authorities
- Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved
- Interact with study participants as directed/required by the protocol and/or study team
- May be responsible for tissue sample work
- Travel between DFCI satellite locations to support all above research activities when cross coverage is needed
- Maintain working knowledge of current regulations, regulatory guidance and or local policies
- May be responsible for preparing and presenting study status regulatory status for satellite site clinical team members at monthly research meetings
KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:
- Excellent organization and communications skills
- Strong interpersonal skills with the ability to effectively interact with all levels of staff and externals contacts
- Must be detail oriented and have the ability to follow-through
- Ability to effectively manage time and prioritize workload
- Must practice discretion and adhere to hospital confidentiality guidelines at all times
- Must have computer skills including the use of Microsoft Office
MINIMUM JOB QUALIFICATIONS:
The position requires a bachelor's degree, with 0 to 1 year of related experience preferred. Experience in a medical, scientific research, or technology-oriented business environment is also preferred. The role requires close to moderate supervision.
SUPERVISORY RESPONSIBILITIES: None
PATIENT CONTACT: Minimal patient contact.
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
EEO Poster
Pay Transparency Statement
The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate's relevant experience, skills and qualifications.
For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).
$48,100.00 - $54,400.00
What Dana-Farber Cancer Institute employees say
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About Dana-Farber Cancer Institute
Sourced by ZipRecruiter
Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.
Industry
Health care and social assistance
Company size
1,001 - 5,000 Employees
Headquarters location
Boston, MA, US
Year founded
1947