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Clinical Research Consortium Jobs (NOW HIRING)

Clinical Research Nurse This Clinical Research Nurse role combines direct patient care with ... Interact regularly with consortium members and participating institutions involved in multi-site ...

Clinical Research Nurse This Clinical Research Nurse role combines direct patient care with ... Interact regularly with consortium members and participating institutions involved in multi-site ...

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Clinical Research Consortium information

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$49K

$107.3K

$189K

How much do clinical research consortium jobs pay per year?

As of Aug 26, 2026, the average yearly pay for clinical research consortium in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a clinical research consortium?

A Clinical Research Consortium is a collaborative partnership of multiple organizations, institutions, or research centers that work together to conduct clinical research studies. These consortia aim to pool resources, expertise, and data to accelerate medical discoveries and improve patient care. By working together, members of a consortium can undertake larger and more complex studies than would be possible individually, often leading to more robust and generalizable results. They also facilitate the sharing of best practices, standardization of protocols, and faster recruitment of study participants.

How does working within a clinical research consortium differ from conducting research in a single institution?

Working within a Clinical Research Consortium involves collaborating with multiple institutions, which allows for larger patient populations, more diverse data, and shared resources. This setup often means frequent cross-institutional communication, standardized protocols, and joint decision-making. While this can present challenges such as coordinating across different organizational cultures and regulatory requirements, it also offers researchers exposure to innovative methodologies and broader networking. Team members typically participate in regular consortium meetings, data sharing, and contribute to multi-site study management.

What are the key skills and qualifications needed to thrive in a clinical research consortium role, and why are they important?

To thrive in a Clinical Research Consortium role, you need strong knowledge of clinical research protocols, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is often required. Excellent collaboration, project management, and communication skills are essential for coordinating among multiple stakeholders and sites. These skills ensure rigorous study conduct, data integrity, and effective collaboration critical for large-scale, multi-center research initiatives.

What is the difference between Clinical Research Consortium vs Clinical Research Coordinator?

AspectClinical Research ConsortiumClinical Research Coordinator
CredentialsVaries; often includes research administration or management experienceTypically requires a bachelor's degree in health or related field; certifications like CCRP are common
Work EnvironmentCollaborative, multi-site research projects, often in academic or industry settingsClinical trial sites, hospitals, or research centers, directly managing participant activities
Employer & Industry UsageResearch institutions, universities, pharmaceutical companiesHospitals, clinics, research sites
Comparison FocusOversees multiple research sites and projects, managing collaborationsManages individual clinical trial activities at a specific site

While both roles are involved in clinical research, a Clinical Research Consortium coordinates multiple research sites and projects, focusing on collaboration and management. In contrast, a Clinical Research Coordinator handles the day-to-day activities at a single research site, ensuring protocol adherence and participant safety.

More about Clinical Research Consortium jobs

What cities are hiring for Clinical Research Consortium jobs?

Cities with the most Clinical Research Consortium job openings:

What states have the most Clinical Research Consortium jobs?

States with the most job openings for Clinical Research Consortium jobs include:

What job categories do people searching Clinical Research Consortium jobs look for?

The top searched job categories for Clinical Research Consortium jobs are:

Infographic showing various Clinical Research Consortium job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Trial Research Monitor - Beat Childhood Cancer Research Consortium

Penn State University

Hershey, PA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 days ago


Penn State University rating

7.8

Company rating: 7.8 out of 10

Based on 104 frontline employees who took The Breakroom Quiz

233rd of 623 rated colleges and universities


Job description

APPLICATION INSTRUCTIONS:
  • CURRENT PENN STATE EMPLOYEE (faculty, staff, technical service, or student), please login to Workday to complete the internal application process. Please do not apply here, apply internally through Workday.
  • CURRENT PENN STATE STUDENT (not employed previously at the university) and seeking employment with Penn State, please login to Workday to complete the student application process. Please do not apply here, apply internally through Workday.
  • If you are NOT a current employee or student, please click "Apply" and complete the application process for external applicants.

Approval of remote and hybrid work is not guaranteed regardless of work location. For additional information on remote work at Penn State, see Notice to Out of State Applicants.
POSITION SPECIFICS
he Beat Childhood Cancer Research Consortium at the Penn State College of Medicine, Hershey, PA, is hiring a full-time Clinical Trial Research Monitor. The Beat Childhood Cancer Research Consortium (BCC) is an international clinical research sponsor and acts as a Contract Research Organization (CRO) of a network of 50+ hospitals across the US and Canada that participate in BCC's investigator-initiated clinical trials.
This job does require travel to BCC hospital sites for monitoring visits approximately every 4-6 weeks.
The ideal candidate will have a strong background in Clinical Trial Management, Human Subjects Research, and IND/IDE regulatory requirements. It is important that the candidate have experience working with a team, multiple Principal Investigators, and Phase I/II clinical trial projects. The candidate must have strong verbal and written communication skills and be able to multi-task while fostering an environment of collaboration and teamwork.
For more information on BCC visit our website: Home | Beat Childhood Cancer (beatcc.org)
BCC Specific Position Roles:
The Clinical Trial Research Monitor is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. This position is the primary contact between the Investigational Sites and BCC Leadership. Key responsibility of this position is ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements and BCC SOPs.
  • Build relationships with Principal Investigators, study coordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited, and smooth management of clinical trials.
  • Foster internal and external relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines.
  • In collaboration with Regulatory teammates, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials.
  • Monitoring of investigational sites as per ICH GCP §5.18 (Monitoring) and the BCC Study Monitoring Plan for each BCC study. This includes all monitoring visit types across all phases of a clinical trial including Site Initiation, Site Monitoring and Site Close Out. Visits may be conducted either onsite or remote as needed.
    • Ensure the rights & wellbeing of trial participants are protected, including consent form checks, patient eligibility confirmation, protocol compliance, investigational drug compliance, and review of Adverse Events/SAEs. Ensure safety issues are reported to BCC promptly.
    • Verify trial data are accurate and complete, ensure CRF data and queries are completed and resolved as per the study timelines documented in the Study Monitoring Plan.
    • Ensure all study drug is appropriately stored, dispensed, accounted for, and reconciled as per the Study Monitoring Plan and the Protocol.
  • Provide guidance to sites to help establish and/or enhance processes for data collection and data management. Educate BCC enrolling sites staff concerning protocols, EDC and regulatory requirements and expectations.

This position will be filled at an Professional, Intermediate Professional depending on the candidate's education and experience. This position requires a Bachelor's Degree and 1+ years of relevant experience or an equivalent combination of education and experience. Additional education and/or experience required for higher level positions.
This is a limited-term position funded for one year from date of hire, with possibility of refunding.
This job requires that you operate a motor vehicle as a part of your job duties. A valid US driver's license and successful completion of a motor vehicle records check will be required in addition to standard background checks.
Employment will require successful completion of background check(s) in accordance with University polices.
The Pennsylvania State University is committed to and accountable for advancing diversity, equity, and inclusion in all of its forms. We embrace individual uniqueness, foster a culture of inclusive excellence that supports both broad and specific diversity initiatives, leverage the educational and institutional benefits of diversity, and engage all individuals to help them thrive. We value inclusive excellence as a core strength and an essential element of our public service mission.
MINIMUM EDUCATION, WORK EXPERIENCE & REQUIRED CERTIFICATIONS
If filled as Research Project Manager - Professional, this position requires:Bachelor's DegreeNo prior relevant work experience required; previous relevant work experience accepted in lieu of education.Required Certifications:NoneIf filled as Research Project Manager - Intermediate Professional, this position requires:Master's Degree1+ years of relevant experience; or an equivalent combination of education and experience acceptedRequired Certifications:None
BACKGROUND CHECKS/CLEARANCES
Penn State does not sponsor or take over sponsorship of a staff employment Visa. Applicants must be authorized to work in the U.S.
SALARY & BENEFITS
The salary range for this position, including all possible grades, is $59,580.00 - $94,980.00.
Salary Structure - Information on Penn State's salary structure
Penn State provides a competitive benefits package for full-time employees designed to support both personal and professional well-being. In addition to comprehensive medical, dental, and vision coverage, employees enjoy robust retirement plans and substantial paid time off which includes holidays, vacation and sick time. One of the standout benefits is the generous 75% tuition discount, available to employees as well as eligible spouses and children. For more detailed information, please visit our Benefits Page.
CAMPUS SECURITY CRIME STATISTICS
Pursuant to the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act and the Pennsylvania Act of 1988, Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters. The ASR is available for review here.
EEO IS THE LAW
Penn State is an equal opportunity employer and is committed to providing employment opportunities to all qualified applicants without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you are unable to use our online application process due to an impairment or disability, please contact 814-865-1473.
Penn State is committed to and accountable for advancing equity, respect, and belonging. We embrace individual uniqueness, as well as a culture of belonging that supports equity initiatives, leverages the educational and institutional benefits of inclusion in society, and provides opportunities for engagement intended to help all members of the community thrive. We value belonging as a core strength and an essential element of the university's teaching, research, and service mission.
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