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Research Monitor Jobs (NOW HIRING)

Headlands Research

Phlebotomist

Portland, OR

$18 - $22.50/hr

Participate in investigator meetings, study teleconferences, and trainings. * Assist with onsite or remote clinical research monitor visits. Requirements: * Bachelor's degree preferred or equivalent ...

Edwards Lifesciences Corporation

$126K - $178K/yr

Providing input on strategic direction on field monitoring of studies and data collection for ... Clinical research certification (ACRP or SoCRA clinical coordinator / CRA certification) * Proven ...

Headlands Research

Medical Assistant

Portland, OR

$18.75 - $24.25/hr

Participate in investigator meetings, study teleconferences, and trainings. * Assist with onsite or remote clinical research monitor visits. Requirements: * Bachelor's degree preferred or equivalent ...

Headlands Research

Phlebotomist

Portland, OR · On-site

$18 - $22.50/hr

Participate in investigator meetings, study teleconferences, and trainings. * Assist with onsite or remote clinical research monitor visits. Requirements: * Bachelor's degree preferred or equivalent ...

Headlands Research

Medical Assistant

Portland, OR · On-site

$18.75 - $24.25/hr

Participate in investigator meetings, study teleconferences, and trainings. * Assist with onsite or remote clinical research monitor visits. Requirements: * Bachelor's degree preferred or equivalent ...

CompoSecure

Research & Data Analyst

Somerset, NJ · On-site

$85K - $100K/yr

The Research & Data Analyst will serve as a key source of market and business intelligence for ... Monitor and report on key trends shaping the financial card, payments, and fintech industries ...

CompoSecure

Research & Data Analyst

Somerset, NJ

The Research & Data Analyst will serve as a key source of market and business intelligence for ... Monitor and report on key trends shaping the financial card, payments, and fintech industries ...

CompoSecure

Research & Data Analyst

Somerset, NJ · On-site

$85K - $100K/yr

The Research & Data Analyst will serve as a key source of market and business intelligence for ... Monitor and report on key trends shaping the financial card, payments, and fintech industries ...

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Research Monitor information

Is CRA better than CRC?

A Research Monitor typically works in clinical research settings, and the roles of CRA (Clinical Research Associate) and CRC (Clinical Research Coordinator) are distinct; CRAs usually oversee multiple sites and monitor trial progress, while CRCs manage day-to-day trial activities at a single site. Neither role is inherently better, but CRAs often require more experience and travel, whereas CRCs focus on patient interaction and data collection.

What is the difference between Research Monitor vs Research Analyst?

AspectResearch MonitorResearch Analyst
Required CredentialsBachelor's degree in related field; certifications optionalBachelor's or master's degree in related field; certifications beneficial
Work EnvironmentMonitoring research activities, ensuring compliance, overseeing data collectionAnalyzing data, preparing reports, interpreting research findings
Employer & Industry UsageResearch institutions, market research firms, academic settingsMarket research firms, financial institutions, consulting firms

Research Monitors primarily oversee research processes and ensure compliance, while Research Analysts focus on analyzing data and producing insights. Both roles require similar educational backgrounds, but their responsibilities differ significantly within the research process.

What are some common challenges faced by Research Monitors when overseeing clinical trials?

Research Monitors often encounter challenges such as ensuring consistent adherence to protocols across multiple sites, managing complex regulatory documentation, and effectively communicating findings to both site staff and sponsors. They must be detail-oriented to identify potential issues in data collection and patient safety while balancing frequent travel and tight timelines. Building strong relationships with site teams and staying current with regulatory changes can help address these challenges and contribute to the success of clinical trials.

What are the key skills and qualifications needed to thrive as a Research Monitor, and why are they important?

To thrive as a Research Monitor, you need a strong understanding of research ethics, regulatory compliance, and clinical trial protocols, often supported by a degree in a health or science field. Familiarity with data management systems, electronic case report forms (eCRFs), and Good Clinical Practice (GCP) certification is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring research integrity and clear reporting. These skills ensure that studies comply with regulations, data is accurate, and participant safety is maintained throughout the research process.

What is the highest paying research job?

The highest paying research jobs are often in specialized fields such as pharmaceutical research, clinical research management, or research director roles, which can offer salaries exceeding $150,000 annually. These positions typically require advanced degrees, extensive experience, and leadership skills, and may involve working in corporate, government, or private research institutions.

Is CRA an entry level job?

A Clinical Research Associate (CRA) role is typically not entry-level and usually requires prior experience in clinical research, monitoring, or related healthcare fields. Entry-level positions may be available for those with relevant internships, certifications, or a background in life sciences, but most CRAs progress into the role after gaining experience. Strong knowledge of Good Clinical Practice (GCP) guidelines and attention to detail are important for success in this position.

What are Research Monitors?

Research Monitors are professionals responsible for overseeing the conduct of research studies to ensure compliance with protocols, regulations, and ethical standards. They play a crucial role in monitoring clinical trials or other research projects by reviewing data, conducting site visits, and verifying that procedures are followed correctly. Research Monitors help protect the integrity of the research and the safety of participants by identifying and addressing any issues that arise during the study. Their work ensures that research results are reliable and that all activities adhere to established guidelines.

How to become a research monitor?

To become a research monitor, candidates typically need a bachelor's degree in a relevant field such as health sciences, social sciences, or research methodology. Experience with data collection, analysis, and familiarity with research protocols or software like SPSS or SAS can be beneficial. Strong attention to detail, organizational skills, and understanding of ethical guidelines are also important for this role.
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Research Monitor jobs near you
Infographic showing various Research Monitor job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, and 3% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.
Clinical Research Nurse

Clinical Research Nurse

Phoenix Children's Hospital

Phoenix, AZ • On-site

Full-time

Posted 23 days ago

Job description

Position Details
Department: PCH-MAIN | Magnet Program
Location: Phoenix
Shift: Mon-Fri, Days, 8am-5pm
Category: Research
Posting #: 1016089
Employee Type: Full-Time
Position Summary
This position provides and coordinates clinical care for research subjects. This position has a central role in assuring participant safety, ongoing maintenance of informed consent, integrity of protocol implementation, and accuracy of data collection, data recording and follow-up. This position also engages in study procedures including administration of investigational drugs, detailed clinical assessments including adverse event assessments, and performing laboratory tests. Additional nursing care may be necessitated by the response of the participant to the study intervention. This position is responsible for study coordination and data management, with a central focus on managing subject recruitment and enrollment, consistency of study implementation, data management and integrity, and compliance with regulatory and institutional requirements and reporting. This position will support the Principal Investigator and Research team for departmental studies under minimal supervision.
Position Duties
  • Provides nursing care to research study patients, including:
    1. Performs and/or schedules medical tests within the scope of nursing licensure including, but not limited to, laboratory tests, vital sign readings, imaging studies, cardiac and/or pulmonary function tests, and psychological evaluations.
    2. Administers study medications and performs patient assessments during clinic visits to determine presence of side effects to medication; notifies principle investigator and responds to findings/issues.
    3. Provides patient education and medical information to study patients and their families to ensure understanding of proper medication dosage, administration and disease treatment.
    4. Documents medical data in patient chart to ensure availability of timely records for decision making.
  • Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), and Good Clinical Practices (GCP) guidelines, including:
    1. Reviews all regulatory requirements to ensure implementation of appropriate methods, practices, and procedures for all research activities in designated area.
    2. Responsible for the completion and submission of documents to the appropriate IRB and institutional committees on an ongoing basis.
    3. Maintains compliance with current and accurate documentation in the regulatory binders as required by regulations and sponsors.
    4. With the principal investigator, explains the study purpose, parameters, and requirements of the studies to the participants.
    5. Coordinates research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
  • Coordinates the process for opening new studies.
    1. Obtains needed background material(s) on proposed research projects; presents findings and information to attending physician/principle investigator.
    2. Completes feasibility questionnaires.
    3. Circulates the confidentiality disclosure and trial agreements to the appropriate parties.
    4. Creates study budgets and works with management to determine financial feasibility and resources necessary to conduct the trial.
    5. Develops work flow procedures for study team based on specific protocol.
  • Completes all tasks required by study sponsors.
    1. Provides regulatory documents to sponsor in timely manner.
    2. Completes case report forms, data entry, and maintains source documentation for all study participants.
    3. Tracks and reports adverse events per sponsor and institutional guidelines.
    4. Coordinates research monitor visits and responds to all data queries.
  • Participates in recruitment and selection of study participants. Coordinates and participates in research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
  • Reviews monthly financial reports, including study participant billing, expenditures, and revenue. Maintains inventory level of all supplies and equipment, initiates requisitions for replacement items, and maintains equipment to provide for continuous operational efficiency.
  • Participates in a variety of professional development programs to ensure ongoing awareness and understanding of most current methodologies, practices, and philosophies as applied to the relevant patient population and research area.
  • Performs miscellaneous job related duties as requested.

Phoenix Children's Mission, Vision, & Values
Mission
To advance hope, healing and the best healthcare for children and their families
Vision
Phoenix Children's will be the leading pediatric health system in the Southwest, nationally recognized for exceptional care, innovative research and advanced medical education.
We realize this vision by:
  • Offering the most comprehensive care across ages, communities and specialties
  • Investing in innovative research, including emerging treatments, tools and technologies
  • Advancing education and training to shape the next generation of clinical leaders
  • Advocating for the health and well-being of children and families
Values
  • We place children and families at the center of all we do
  • We deliver exceptional care, every day and in every way
  • We collaborate with colleagues, partners and communities to amplify our impact
  • We set the standards of pediatric healthcare today, and innovate for the future
  • We are accountable for making the highest quality care accessible and affordable
Phoenix Children's Hospital logo

About Phoenix Children's Hospital

Sourced by ZipRecruiter

Phoenix Children's Hospital, located in Phoenix, AZ, is a prominent establishment within the healthcare industry. Known for its commitment to pediatric healthcare, the hospital provides a vast range of services catering to the unique health needs of children. Originally founded in 1983, Phoenix Children's Hospital prides itself on being one of the largest and most respected children's hospitals in the country. Guided by its mission–"to provide hope, healing and the best healthcare for children and their families"–the hospital holds strong on its core values of family-centered care, excellence in clinical care, innovation, and stewardship.

Industry

Health care and social assistance

Company size

1,001 - 5,000 Employees

Headquarters location

Phoenix, AZ, US

Year founded

1983

Social media

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