The CVD is looking for a Contractual Clinical Research Nurse to join our team. This is a Full-Time, Contractual position. Benefits: Contingent Category II UMB offers acomprehensive benefits ...
The CVD is looking for a Contractual Clinical Research Nurse to join our team. This is a Full-Time, Contractual position. Benefits: Contingent Category II UMB offers acomprehensive benefits ...
Facilitates preparation and execution of contractual agreements with pharmaceutical, biotechnology ... clinical trials contract negotiation highly preferred 3 years of research experience preferred ...
Facilitates preparation and execution of contractual agreements with pharmaceutical, biotechnology ... clinical trials contract negotiation highly preferred 3 years of research experience preferred ...
Contractual Nurse, Clinical Research
Baltimore, MD · On-site
$87 - $97/hr
This is a Full-Time, Contractual position. Benefits: Contingent Category II UMB offers a ... Recruits research and clinical trial subjects. Interacts withsubject participants that include ...
Contractual Nurse, Clinical Research
Baltimore, MD · On-site
$87 - $97/hr
This is a Full-Time, Contractual position. Benefits: Contingent Category II UMB offers a ... Recruits research and clinical trial subjects. Interacts withsubject participants that include ...
Coronary Structural Heart Clinical is looking for an enthusiastic, motivated candidate to be a contract Clinical Research Specialist in our dynamic environment. The incumbent has responsibility for ...
Coronary Structural Heart Clinical is looking for an enthusiastic, motivated candidate to be a contract Clinical Research Specialist in our dynamic environment. The incumbent has responsibility for ...
In-house Sr Clinical Research Associate
San Diego, CA · On-site
$60 - $75/hr
A clinical-stage biopharmaceutical company in San Diego, California is seeking an experienced Contract Clinical Research Associate (CRA) to support ongoing clinical trials. This is an in-house ...
In-house Sr Clinical Research Associate
San Diego, CA · On-site
$60 - $75/hr
A clinical-stage biopharmaceutical company in San Diego, California is seeking an experienced Contract Clinical Research Associate (CRA) to support ongoing clinical trials. This is an in-house ...
Clinical Research Coordinator (Contract)
Edinburg, TX · On-site
$17.50 - $23.25/hr
The Clinical Research Coordinator will manage the day-to-day operations of assigned clinical trials and ensure that pre-established work scope, study protocol, and regulatory requirements are ...
Clinical Research Coordinator (Contract)
Edinburg, TX · On-site
$17.50 - $23.25/hr
The Clinical Research Coordinator will manage the day-to-day operations of assigned clinical trials and ensure that pre-established work scope, study protocol, and regulatory requirements are ...
Assists other contract service providers, military commanders and community agencies in the ... Rather, salary will be set based on experience, geographic location and possibly contractual ...
Assists other contract service providers, military commanders and community agencies in the ... Rather, salary will be set based on experience, geographic location and possibly contractual ...
Assists other contract service providers, military commanders and community agencies in the ... Rather, salary will be set based on experience, geographic location and possibly contractual ...
Assists other contract service providers, military commanders and community agencies in the ... Rather, salary will be set based on experience, geographic location and possibly contractual ...
... and contractual expertise. This position is a position of leadership whose main purpose is to ... In-depth and extensive knowledge of clinical research contracts and grants, clinical trials ...
... and contractual expertise. This position is a position of leadership whose main purpose is to ... In-depth and extensive knowledge of clinical research contracts and grants, clinical trials ...
... site and Clinical Research Organization (CRO) management, data review, and study reporting ... negotiates contracts and budgets with sites and vendors and presents to the project team for ...
... site and Clinical Research Organization (CRO) management, data review, and study reporting ... negotiates contracts and budgets with sites and vendors and presents to the project team for ...
Program Lead, Clinical Research
Manhattan, NY · On-site
$84.58 - $101.22/hr
Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...
Program Lead, Clinical Research
Manhattan, NY · On-site
$84.58 - $101.22/hr
Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...
Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...
Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...
Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...
Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...
Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...
Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job title: Contract Clinical Operations Lead Location:Cambridge,MA Duration: 6+ months (Possibility of extension ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job title: Contract Clinical Operations Lead Location:Cambridge,MA Duration: 6+ months (Possibility of extension ...
This position independently coordinates complex regulatory, contractual, financial, and operational ... The role oversees Clinical Research Trial contract workflows, supports negotiations, manages ...
This position independently coordinates complex regulatory, contractual, financial, and operational ... The role oversees Clinical Research Trial contract workflows, supports negotiations, manages ...
... human research, human resources, contracts and grants) and elsewhere (industry sponsors ... and contractual expertise. This position is a position of leadership whose main purpose is to ...
... human research, human resources, contracts and grants) and elsewhere (industry sponsors ... and contractual expertise. This position is a position of leadership whose main purpose is to ...
Clinical Research Financial Analyst
Irvine, CA · On-site
$75K - $85K/yr
The Irvine Clinical Research site network is the largest of its kind on the West Coast. With five ... High attention to detail with the ability to detect errors in complex contracts * Self-starter ...
Clinical Research Financial Analyst
Irvine, CA · On-site
$75K - $85K/yr
The Irvine Clinical Research site network is the largest of its kind on the West Coast. With five ... High attention to detail with the ability to detect errors in complex contracts * Self-starter ...
The Irvine Clinical Research site network is the largest of its kind on the West Coast. With five ... High attention to detail with the ability to detect errors in complex contracts * Self-starter ...
Quick apply
The Irvine Clinical Research site network is the largest of its kind on the West Coast. With five ... High attention to detail with the ability to detect errors in complex contracts * Self-starter ...
Clinical Research Financial Analyst
$75K - $85K/yr
The Irvine Clinical Research site network is the largest of its kind on the West Coast. With five ... High attention to detail with the ability to detect errors in complex contracts * Self-starter ...
Clinical Research Financial Analyst
$75K - $85K/yr
The Irvine Clinical Research site network is the largest of its kind on the West Coast. With five ... High attention to detail with the ability to detect errors in complex contracts * Self-starter ...
Contractual Contract Clinical Research information
See salary details
$17.79 - $20.19
10% of jobs
$22.60 is the 25th percentile. Wages below this are outliers.
$20.19 - $22.60
15% of jobs
$22.60 - $25
18% of jobs
The median wage is $25.99 / hr.
$25 - $27.40
18% of jobs
$29.27 is the 75th percentile. Wages above this are outliers.
$27.40 - $29.81
19% of jobs
$29.81 - $32.21
9% of jobs
$32.21 - $34.62
4% of jobs
$34.62 - $37.02
1% of jobs
$37.02 - $39.42
1% of jobs
$39.42 - $41.83
2% of jobs
$41.83 - $44.23
3% of jobs
$17
$27
$44
How much do contractual contract clinical research jobs pay per hour?
What is the difference between Contractual Contract Clinical Research vs Contractual Clinical Research Coordinator?
| Aspect | Contractual Contract Clinical Research | Contractual Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires a degree in life sciences, nursing, or related field; certifications like CCRP are common | Requires similar credentials; often holds a degree in health sciences or related field; certifications like CCRP are advantageous |
| Work Environment | Conducts clinical trials, manages study protocols, and liaises with sponsors in research settings | Coordinates daily clinical trial activities, enrolls patients, and ensures protocol adherence at research sites |
| Employer & Industry Usage | Used by pharmaceutical companies, CROs, and research institutions for contractual research roles | Commonly employed by hospitals, research centers, and clinical trial sites |
Both roles involve clinical research but differ mainly in scope and responsibilities. Contractual Contract Clinical Research professionals often oversee entire studies or projects, while Contractual Clinical Research Coordinators focus on day-to-day trial coordination at research sites. Understanding these differences helps in choosing the right career path or job opportunity.
What cities are hiring for Contractual Contract Clinical Research jobs?
Cities with the most Contractual Contract Clinical Research job openings:
What states have the most Contractual Contract Clinical Research jobs?
States with the most job openings for Contractual Contract Clinical Research jobs include:
What job categories do people searching Contractual Contract Clinical Research jobs look for?
The top searched job categories for Contractual Contract Clinical Research jobs are:

Contractual Nurse, Clinical Research
Baltimore, MD • On-site
7.7
Based on 13 frontline employees who took The Breakroom Quiz
264th of 623 rated colleges and universities
People enjoy working here
Good employer
Respectful managers
Uninterrupted breaks
Other
Medical, Life, Retirement, PTO
Posted 20 days ago
Job description
The University of Maryland, Baltimore (UMB), Center for Vaccine Development and Global Health (CVD)brings together more than four decades of innovative and life-saving research on vaccines and infectious diseases. The CVD is looking for aContractual Clinical Research Nurseto join our team. This is a Full-Time, Contractual position. Benefits: Contingent Category II UMB offers acomprehensive benefits packagethat prioritizes wellness, work/life balance, and professional development, along withadditional exciting perksthat employees can take advantage of. Contingent Category II staff receive a generous leave package that includes over 2 weeks of vacation each year, paid holidays, sick time, and time for community service; subsidized comprehensive health insurance and supplemental retirement options; professional learning and development programs; limited tuition remission for employees enrolled at UMB; life insurance and long-term disability; and flexible work schedules and teleworking options (if applicable per job). *UMB is a public university and constituent institution of the University System of Maryland. All employees are expected to work primarily physically within the State of Maryland. * Primary Duties: * Manages operations of one or more research studies or clinical trial protocols requiring the expertise and care of a Registered Nurse. Instructs and counsels patients in research procedures, administers treatment procedures, monitors patients during procedures, and analyzes patient data. Develops and tracks workflow policies, recruitment strategy, and progress through the duration of the research study or clinical trial. Collaborate with Principal Investigators and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials. Reviews and recommends proposed research study and clinical trial protocols to evaluate factors such as sample collection process, facility location, data management plans, and potential subject risks. * Recruits research and clinical trial subjects. Interacts with subject participants that include eligibility screening, recruitment, and enrollment. Ensure informed consent is properly secured and documented, counseling, and obtaining patient medical history. Serves as a patient advocate throughout the research study or clinical trial. Develops and conducts patient and family education. * Instructs and counsels patients in research procedures and administer treatment procedures. Manage patient care in compliance with the research study or clinical trial protocol requirements. Monitors subject condition while ensuring safety and maintaining confidentiality. Identifies patient problems and makes adjustments to care plans. * Develops, recommends, and implements policies and procedures and/or methods of clinical research to meet changing needs and requirements and enforce standards. Performs Institutional Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPAA) protocol development and ensure compliance of research operations with protocols and all relevant local, federal, and state regulatory and institutional policies. * Develops and prepares study or research related documentation such as protocol worksheets, procedural manuals, adverse event reports, case report forms, and institutional review board documents. Responsible for developing and producing custom and routine reports. Conducts quality assurance audits on data and regulatory documentation. Identifies protocol problems, informs investigators, and assists in problem resolution efforts. Recommend modifications and adjustments to care plans. * Administer and implement treatment procedures or drugs, monitors and studies their effects, and conducts subject medical evaluations. Obtains biologic tissue and blood samples as necessary and collects information through interviews, questionnaires, test results, and charts. * Manages the collection of complex research study or clinical trial data. Develops methods for collection, database storage, tracking, analysis, and interpretation of data. Prepares study and research related documentation. * Assist in monitoring study, clinical trial, or unit budget and compliance. May identify potential research study and clinical trial opportunities. Assist in writing research grants, publications in medical and nursing literature, study materials, brochures, and correspondence. * Serves as a liaison to other departments, outside organizations, government agencies, and sponsors to promote effective and efficient operation and use of resources. Attends research study or clinical trial related meetings, conferences, and teleconferences, as well as participating in any additional planning and development related activities. * Provide guidance and direction to staff engaged in clinical research or trials to ensure compliance with protocols and overall clinical objectives. Continuously educates and trains personnel on compliance and protocol. * Perform other duties as assigned. *Education:*Bachelor's degree. Preference in Nursing or other discipline appropriate to the position. *Experience:*Three (3) years’ experience nursing, clinical, or in a relevant research specialization related to the position. *Supervisory Experience:*N/A *Certification/Licensure:*Current Maryland license in good standing issued by the Maryland Board of Nursing to practice as a registered nurse or a multistate licensure privilege to practice as a registered nurse in Maryland or appropriate federal district licensure where research is conducted. *Other:*Certification from Association of Clinical Research Professionals or Society of Clinical Research Associates preferred May require training related to occupational safety and health, environmental compliance, shipping of hazardous materials and/or ionizing radiation. Except for qualifications established by law, additional related experience and formal education in which one has gained the knowledge, skills, and abilities required for full performance of the work of the job class may be substituted for the education or experience requirement on a year-for-year basis with 30 undergraduate college credits being equivalent to one year of related experience. In instances where specific education and/or experience is required only directly related education and/or experience may be substituted. Knowledge, Skills, Abilities: Knowledge of position requirements. Knowledge of all applicable requirements, regulations, and laws. Skill in effective use of applicable technology/systems. Ability to effectively communicate both verbal and written thoughts, ideas, and facts. Ability to work cooperatively with others and independently. Ability to demonstrate, understand, apply, and adhere to the UMB Core Values of Respect and Integrity, Well-being and Sustainability, Equity and Justice, and Innovation and Discovery. *Hiring Range: $87,000 - $97,000, Commensurate with education and experience * UMB is committed to cultivating a diverse and inclusive workforce and is proud to be an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, ancestry or national origin, sex, pregnancy or related conditions, sexual orientation, gender identity or expression, genetic information, physical or mental disability, marital status, protected veteran's status, or any other legally protected classification. If you anticipate needing a reasonable accommodation for a disability under the Americans with Disabilities Act (ADA), during any part of the employment process, please submit aUMB Job Applicant Accommodation Request. You may also contactleave_and_accom@umaryland.edu Please note that only inquiries concerning an ADA request for reasonable accommodation will be responded to from this email address. The University of Maryland, Baltimore prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to the Title IX Coordinator. Read theUMB Notice of Non-Discriminationfor more information. Job: *Reg or CII Exempt Staff Organization: *School of Medicine Title: *Contractual Nurse, Clinical Research * Location: null Requisition ID: 260000QI
About University of Maryland, Baltimore
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1,001 - 5,000 Employees
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Baltimore, MD, US
Year founded
1807
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