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Full Time Research Ethics Jobs (NOW HIRING)

The US Oncology Network

Research Assistant

Woodbridge, VA · On-site

$19 - $26.25/hr

... seeking a Full Time Research Assistant for our Woodbridge office. Under direct supervision ... Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and ...

The US Oncology Network

Research Assistant

Fairfax, VA

$19 - $26.25/hr

... is seeking a Full Time Research Assistant for our Fairfax office. Under direct supervision ... Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and ...

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Full Time Research Ethics information

What is a full time research ethics position?

Full Time Research Ethics positions involve overseeing, developing, and ensuring compliance with ethical standards in research activities within organizations such as universities, hospitals, or research institutions. These professionals help review research proposals, provide training on ethical practices, and ensure that research involving humans or animals adheres to legal and institutional guidelines. They may also participate in ethics committees, conduct audits, and advise researchers on best practices to protect participants and maintain integrity in scientific work.

What are the key skills and qualifications needed to thrive as a full time research ethics professional?

To thrive as a Full Time Research Ethics professional, you need expertise in ethical theory, research methodologies, and relevant regulatory frameworks, often supported by an advanced degree in ethics, law, or a related field. Familiarity with institutional review board (IRB) protocols, compliance management systems, and federal regulations such as the Common Rule is typically required. Strong analytical thinking, attention to detail, and effective communication are vital soft skills for evaluating proposals and guiding researchers. These skills and qualifications ensure the protection of research participants, maintain institutional integrity, and uphold legal and ethical standards in research.

What are some typical challenges faced in a full time research ethics role, and how can they be addressed?

Professionals in research ethics often navigate complex ethical dilemmas, such as balancing participant safety with research goals and ensuring regulatory compliance. One common challenge is handling conflicts between researchers' objectives and ethical guidelines, which requires strong communication and negotiation skills. Staying current with evolving regulations and fostering collaboration across departments are also essential. Building a culture of ethical awareness and providing ongoing training can help address these challenges and promote responsible research practices.
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Full Time Research Ethics jobs near you
Infographic showing various Full Time Research Ethics job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 87% Full Time, 9% Part Time, and 2% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.

Clinical Research Coordinator 3

The University of Miami

Miami, FL • On-site

$23.25 - $30.75/hr

Full-time

Medical, Dental

Re-posted 28 days ago

University Of Miami rating

7.7

Company rating: 7.7 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

260th of 617 rated colleges and universities

Job description

Current Employees:
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.
The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 3 to work at the UHealth campus in Miami, Fl.
CORE JOB SUMMARY
The Clinical Research Coordinator 3 serves as experienced clinical research professional responsible for providing leadership in the planning, implementing, monitoring, and evaluating of multiple clinical research protocols. This role manages multiple studies' daily operations, carries out study coordination duties from protocol development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study's integrity, and mentors less experienced Clinical Research Coordinators. The incumbent monitors and maximizes adherence to research standards and regulatory guidelines and approved operational procedures, works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, manages study-related administrative and human resources tasks, facilitates across-the-board flow of information, and orchestrates study activities and personnel.
CORE JOB FUNCTIONS
  • Coordinates the implementation of multiple complex clinical research protocols.
  • Develops SOPs and templates with guidance from the PI/Clinical Research Manager.
  • Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual.
  • Manages sample processing, packing, and shipping according to protocol, applicable standards, and regulations.
  • Plans and operationalizes strategies to monitor, document, report, and follow-up on unanticipated occurrences and protocol deviations. Develops and implements preventive/corrective actions.
  • Develops, disseminates, and assures adherence to study-related clinical research best practices/scientific manuals.
  • Assumes leadership in protocol implementation and study progress, keeping investigators apprised of study progress.
  • Provides leadership in identifying and working through ethical conflicts arising during protocol implementation and refers these conflicts to the Research Ethics Team for consults as needed.
  • Organizes/manages site visits and internal/external auditing activities as assigned.
  • Coordinates research team meetings; assures communications across-the-board.
  • Assures synchronization of study visits/procedures/ clinical tests with data collection schedules, established time-points; manages progress of study participants through protocol; expedites overall study progression.
  • Coordinates the compilation of information needed for research reports; peer-reviewed publications; develops strategies to disseminate information to clinical personnel, professional audiences and stakeholders.
  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.
  • This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.

CORE QUALIFICATIONS
Education: Bachelor's degree in relevant field required
Certification and Licensing:
Current Research Coordinator certification by the Association of Clinical Research Professionals or Society of Clinical Research Associates for a minimum of 6 months. If you do not have the certification, you will have 6 months to obtain it.
Experience: Minimum 4 years of relevant experience required
Knowledge, Skills and Attitudes:
• Skill in collecting, organizing and analyzing data.
• Ability to recognize, analyze, and solve a variety of problems.
• Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
• Ability to process and handle confidential information with discretion.
• Ability to work independently and/or in a collaborative environment.
DEPARTMENT SPECIFICS:
The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Principal Investigator, and Clinical Research Manager. The CRC provides operational and administrative support in the management of patients accrued to multiple research protocols to assure subjects' safety and regulatory compliance. The CRC is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, Standard Operating Procedures and all applicable regulations and guidelines and ensuring effective data flow associated with research protocols.
The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.
Job Status:
Full time
Employee Type:
Staff

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About University of Miami

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The University of Miami, located in the beautiful Coral Gables, Florida, is a comprehensive, private research institution in the United States. Operating within the higher education industry, the institution offers a multitude of degree programs spanning over 180 majors and program through its 12 colleges. The University was founded in 1925 with the mission to disseminate knowledge, transform lives, and change the world - a mission it has held faithfully to this day. Notably, the University of Miami has gained global recognition for its commitment to research and innovation, with over $324 million in research and sponsored project funding awarded annually.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Coral Gables, FL, US

Year founded

1925

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