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Clinical research • usa

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Assistant Clinical Research Coordinator / Clinical Research Coordinator

Assistant Clinical Research Coordinator / Clinical Research Coordinator

UC Davis Health SystemSacramento, CA, United States
[job_card.full_time]
Under the direct supervision of the Clinical Research Supervisor , Office of Clinical Research , the Assistant Clinical Research Coordinator (ACRC) supports the clinical research efforts of the Can...[show_more][last_updated.last_updated_variable_hours]
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Research Administrator II (Clinical Research)

Research Administrator II (Clinical Research)

Joslin Diabetes CenterBoston, MA, United States
[job_card.full_time]
Senior Research Administrator (Research Administrator II).Pre and Post award support to Joslin investigators for complex Clinical Research awards including federal grants and subcontracts, foundati...[show_more][last_updated.last_updated_variable_days]
Clinical Research Associate

Clinical Research Associate

Zachary Piper SolutionsMadison, Wisconsin, US
[job_card.full_time]
Responsibilities of the Clinical Research Associate:.Oversee the development and execution of the clinical trial plans and protocols for Phase I-IV.Maintain documentation and data evaluations.Work ...[show_more][last_updated.last_updated_30]
Clinical - Clinical Research

Clinical - Clinical Research

All Medical PersonnelLos Angeles, CA
[job_card.full_time]
Serve as the primary liaison between the site, study participants, investigators, and sponsors.Coordinate and conduct study visits per protocol, ensuring accurate and timely data collection and doc...[show_more][last_updated.last_updated_30]
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Clinical Research Assistant or Clinical Research Coordinator

Clinical Research Assistant or Clinical Research Coordinator

MedixMurrieta, CA, United States
[job_card.full_time]
Coordinate and manage complex activities throughout the start-up, conduct, and close-out phases of clinical pharmaceutical and device research studies.Ensure timely, accurate, and objective data co...[show_more][last_updated.last_updated_variable_days]
Supv, Clinical Research

Supv, Clinical Research

AdventHealth Orlando SupportOrlando, FL, US
[job_card.full_time]
Joining AdventHealth is about being part of something bigger.It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit....[show_more][last_updated.last_updated_variable_days]
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Clinical Research Coordinator - Stephenson Clinical Research

Clinical Research Coordinator - Stephenson Clinical Research

Beth Israel Lahey HealthBoston, MA, United States
[job_card.full_time]
When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives.Responsible for screening research subjects for participation in clinical research pr...[show_more][last_updated.last_updated_variable_days]
Clinical Research Assistant

Clinical Research Assistant

Perelman School of Medicine University of PennsylvaniaMed Sch Richards Building, 5th Floor, US
[job_card.full_time]
The Perelman School of Medicine at the University of Pennsylvania is the oldest and one of the finest medical schools in the United States.Penn is rich in tradition and heritage and at the same tim...[show_more][last_updated.last_updated_30]
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Clinical Research Associate/Clinical Research Monitor

Clinical Research Associate/Clinical Research Monitor

System OneFort Valley, VA, United States
[job_card.full_time]
Job Title: Clinical Research Associate/Clinical Research Monitor.Location: Ft Detrick, Virginia.Contractor Work Model: Hybrid (1-2days onsite).Security Clearance: Must be a US Citizen with the abil...[show_more][last_updated.last_updated_variable_days]
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Clinical Research Scientist

Clinical Research Scientist

InsideHigherEdBaltimore, Maryland, United States
[job_card.full_time]
School of Medicine - Clinical Departments.[show_more][last_updated.last_updated_30]
Clinical Research Associate - Clinical Research Coordinator Experience

Clinical Research Associate - Clinical Research Coordinator Experience

MEDPACECincinnati, OH, United States
[job_card.full_time]
Medpace is a full-service clinical contract research organization (CRO).We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.Our mi...[show_more][last_updated.last_updated_30]
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Research Administrator II (Clinical Research)

Research Administrator II (Clinical Research)

Harvard UniversityBoston, MA, United States
[job_card.full_time]
Senior Research Administrator (Research Administrator II).Pre and Post award support to Joslin investigators for complex Clinical Research awards including federal grants and subcontracts, foundati...[show_more][last_updated.last_updated_variable_days]
Clinical Research Analyst

Clinical Research Analyst

Digital InfuzionRockville, MD, US
[job_card.full_time]
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We believe that by equipping researchers with rapid insights and providers with tailored, on-demand data, we can help people lead better, healthier lives.At Digital Infuzion, we harness innovative ...[show_more][last_updated.last_updated_variable_days]
Clinical Research Coordinator

Clinical Research Coordinator

Alcanza Clinical ResearchClearwater, Florida, US
[job_card.full_time]
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Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico.We have established a strong pr...[show_more][last_updated.last_updated_variable_days]
Clinical Research Coordinator - NCRI Clinical Research

Clinical Research Coordinator - NCRI Clinical Research

Massachusetts General HospitalBoston, MA, US
[job_card.full_time]
Clinical Research Coordinator - NCRI Clinical Research-(3293430).GENERAL SUMMARY/ OVERVIEW STATEMENT:.Working as a part of the Site at the Neurological Clinical Research Institute (NCRI), and worki...[show_more][last_updated.last_updated_30]
Clinical Research Associate/Clinical Research Monitor

Clinical Research Associate/Clinical Research Monitor

1200 The General Hospital CorporationMA,Boston
[job_card.full_time]
Site: The General Hospital Corporation.Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to a...[show_more][last_updated.last_updated_variable_days]
Clinical Research Nurse

Clinical Research Nurse

Piper CompaniesPhiladelphia, PA
[job_card.full_time]
Piper Clinical Solutions is actively seeking clinical research nurses for a large research center in Philadelphia PA.This position is working Monday through Friday 9am to 5pm with flexibility to wo...[show_more][last_updated.last_updated_30]
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Clinical Research Assistant

Clinical Research Assistant

LifespanProvidence, RI, United States
[job_card.full_time]
Under the general supervision of the Principal Investigator(s) and Clinical Research Coordinator, assist in acquisition and analysis of patient information for multiple clinical research projects.I...[show_more][last_updated.last_updated_variable_days]
Clinical Research Associate

Clinical Research Associate

ICONRemote, Missouri
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[job_card.permanent]
Clinical Research Associate - Oncology - Missouri.ICON plc is a world-leading healthcare intelligence and clinical research organization.We’re proud to foster an inclusive environment driving innov...[show_more][last_updated.last_updated_variable_days]
Assistant Clinical Research Coordinator / Clinical Research Coordinator

Assistant Clinical Research Coordinator / Clinical Research Coordinator

UC Davis Health SystemSacramento, CA, United States
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  • [job_card.full_time]
[job_card.job_description]
MED: Cancer Center

CRC Ast:

Under the direct supervision of the Clinical Research Supervisor , Office of Clinical Research , the Assistant Clinical Research Coordinator (ACRC) supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management for low to medium complexity cancer-related protocols according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures. The incumbent may assist with coordinating care for subjects enrolled on Phase I trials who have entered a lower complexity maintenance part of the trial.

CRC:

The Clinical Research Coordinator (CRC) reports to the Clinical Research Supervisor, Office of Clinical Research, and supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management for medium to high complexity cancer protocols according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures. #CA-SB

Apply By Date 3/26/2026 by 11:59pm

Minimum Qualifications - For full consideration, applicants are encouraged to upload license and/or certification if required of the position

CRC Ast:
  • High School graduation or GED equivalent and/or equivalent experience/training and/or demonstrated skills to successfully perform the assigned duties and responsibilities.
  • Minimum 1-year relevant experience
  • Knowledge and understanding of disease processes as applied to human clinical research.
  • Knowledge of clinical research trials regulations (e.g., Food and Drug Administration [FDA] and Office for Human Research Protections [OHRP]) is essential.
  • Knowledge of basic anatomy, medical terminology and ability to interpret physicians' notes, medical records, laboratory and scan results.
  • Working knowledge with Microsoft Office Suite: Word, Excel, Outlook, Access, etc.
  • Tracking and recordkeeping experience or skills.
  • Analytical skills to evaluate information, changes in practices and procedures, formulate logical and objective conclusions
  • Demonstrate oral communication and interpersonal skills to correspond effectively with the public, co-workers, physicians, patients, caregivers, clinic staff and other health care professionals.
  • Display organizational skills and attention to detail so that large volumes of records can be accurately maintained to accomplish a task or goal in a timely manner.
  • Display writing skills including ability to compose reports and correspondence while utilizing correct grammar, spelling and punctuation as well as clearly documenting research data onto forms.
  • Ability to work independently and/or cooperatively as a team member in a diverse workforce.
  • Ability to work occasional overtime as work demands.
  • Ability to travel on occasion.
Preferred Qualifications
  • Previous experience coordinating clinical trials.
  • Previous experience working in a cancer center.
CRC : all the minimum requirements of a CRC Ast and the below
  • At least 2 years clinical research coordinator experience.
  • Knowledge of regulatory processes as well as a working knowledge of data management activities as applied to clinical trial coordination.
  • Demonstrates good judgement and ability to think critically.
  • Certification by the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP)
  • Bachelor's degree, preferably in the sciences or health related field.
  • Previous oncology-related clinical research experience.
Key Responsibilities

CRC Ast:
  • 4 0% - Study Coordination
  • 40% - Data Coordination
  • 15% - Quality Control
  • 5% - Other
CRC:
  • 60% - Study Coordination
  • 25% - Data Coordination
  • 10% - Quality Control
  • 5% - Other
Department Overview

The UC Davis Comprehensive Cancer Center (UCDCCC) is a campus-wide multidisciplinary matrix organization whose mission is to reduce the burden of cancer among the diverse populations in our community and beyond through bidirectional engagement and transdisciplinary collaborations that enhance our understanding of cancer, inform new ways to prevent and treat cancer, and prepares a committed and inclusive workforce. The Office of Clinical Research (OCR) is the centralized office for clinical research operations within UCDCCC. The OCR services support the entire lifecycle of cancer-related clinical research protocols. These include support for development and implementation of clinical trials, quality control of clinical research operations, and training and education services.

Department Specific Job Scope

The incumbent is responsible for supporting and coordinating all aspects of cancer-related trials for protocol specific requirements, research procedures, research chart preparation, data collection and entry, and record keeping. Attends clinic to assist the Investigators with recruitment, screening, consenting, administering questionnaires, answer research patient questions, schedule appointments, etc.

Serve as the liaison to sponsors, governing agencies and facilitate transmission of verbal and written communication to national cooperative oncology groups, pharmaceutical companies and other research entities as needed. The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, including attending Disease Team (DT) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors.

In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI).

POSITION INFORMATION
  • Salary or Pay Range: CRC Ast: $31.38 - $50.53, CRC: $34.62 - $55.67
  • Salary Frequency: Hourly
  • Salary Grade: 102, 101
  • UC Job Title: CLIN RSCH CRD AST, CLIN RSCH CRD
  • UC Job Code: 009336, 009335
  • Number of Positions: 2 (1 OF 2)
  • Appointment Type: Staff: Career
  • Percentage of Time: 100
  • Shift (Work Schedule): Mon-Fri 8a - 5p
  • Location: Facilities Support Srvcs Bldg (HSP068)
  • Union Representation: RX-Research Professionals
  • Benefits Eligible: Yes
  • This position is 100% on-site
Benefits

Outstanding benefits and perks are among the many rewards of working for the University of California. UC Davis offers a full range of benefits, resources and programs to help you bring your best self to work, as well as to help you and your family achieve your health, wellness, financial and career goals. Learn more about the benefits below and eligibility rules by visiting either our handy Benefits Summary for UC Davis Health Employees or Benefits Summary for UC Davis Employees and our Benefits Page .

If you are represented by a union, benefits are negotiated between the University of California (UC) and your union and finalized in a contract. Read your bargaining unit's employment contract, stay abreast of current negotiations and learn about collective bargaining at UC: https://ucnet.universityofcalifornia.edu/labor/bargaining-units/index.html
  • High quality and low-cost medical plans to choose from to fit your family's needs
  • UC pays for Dental and Vision insurance premiums for you and your family
  • Extensive leave benefits including Pregnancy and Parental Leave, Family & Medical Leave
  • Paid Holidays annually as stipulated in the UC Davis Health Policies or Collective Bargaining Agreement
  • Paid Time Off/Vacation/Sick Time as stipulated in the UC Davis Health Policies or Collective Bargaining Agreement
  • Continuing Education (CE) allowance and Education Reimbursement Program as stipulated in the UC Davis Health Policies or Collective Bargaining Agreement
  • Access to free professional development courses and learning opportunities for personal and professional growth
  • WorkLife and Wellness programs and resources
  • On-site Employee Assistance Program including access to free mental health services
  • Supplemental insurance offered including additional life, short/long term disability, pet insurance and legal coverage
  • Public Service Loan Forgiveness (PSFL) Qualified Employer & Student Loan Repayment Assistance Program for qualified roles
  • Retirement benefit options for eligible roles including Pension and other Retirement Saving Plans. More information on our retirement benefits can be found here
Physical Demands
  • Standing - Occasional Up to 3 Hours
  • Walking - Occasional Up to 3 Hours
  • Sitting - Frequent 3 to 6 Hours
  • Lifting/Carrying 0-25 Lbs - Occasional Up to 3 Hours
  • Pushing/Pulling 0-25 Lbs - Occasional Up to 3 Hours
  • Bending/Stooping - Occasional Up to 3 Hours
  • Squatting/Kneeling - Occasional Up to 3 Hours
  • Twisting - Occasional Up to 3 Hours
  • Reaching overhead - Occasional Up to 3 Hours
  • Keyboard use/repetitive motion - Frequent 3 to 6 Hours
Mental Demands
  • Sustained attention and concentration - Frequent 3 to 6 Hours
  • Complex problem solving/reasoning - Occasional Up to 3 Hours
  • Ability to organize & prioritize - Frequent 3 to 6 Hours
  • Communication skills - Frequent 3 to 6 Hours
  • Numerical skills - Occasional Up to 3 Hours
  • Constant Interaction - Frequent 3 to 6 Hours
  • Customer/Patient Contact - Frequent 3 to 6 Hours
  • Multiple Concurrent Tasks - Frequent 3 to 6 Hours
Work Environment

UC Davis is a smoke and tobacco free campus effective January 1, 2014. Smoking, the use of smokeless tobacco products, and the use of unregulated nicotine products (e-cigarettes) will be strictly prohibited on any UC Davis owned or leased property, indoors and outdoors, including parking lots and residential space.

Ability to work occasional overtime as work demands. Ability to travel on occasion.

Special Requirements - Please contact your recruiter with questions regarding which activities apply by position
  • This is a critical position, as defined by UC Policy and local procedures, and as such, employment is contingent upon clearing a criminal background check(s) and may include drug screening, medical evaluation clearance and functional capacity assessment
  • This position is designated as a mandated reporter under CANRA and UC policy, and employment is contingent on compliance with applicable policies, procedures and training requirements
Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.

A Culture of Opportunity and Belonging

At UC Davis, we're committed to solving life's most urgent challenges and building a healthier, more resilient world. We believe in growing through every challenge, continually striving to improve, and welcoming new perspectives that strengthen our community. We recognize that a vibrant and innovative organization values both individual strengths and shared purpose. The best ideas often emerge when people with different experiences come together.

As you consider joining UC Davis, we invite you to explore our Principles of Community , our Clinical Strategic Plan and strategic vision for research and education. We believe you belong here. The University of California, Davis is an Equal Opportunity Employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status.

To view the University of California's Anti-Discrimination Policy, please visit: https://policy.ucop.edu/doc/1001004/Anti-Discrimination

Because we want you to feel seen and valued, our recruitment process at UC Davis supports openness and authenticity. Research shows that some individuals hesitate to apply unless they meet every qualification. You may be an excellent fit for this role-or the next one. We encourage you to apply even if your experience doesn't match every listed requirement. #YouBelongHere

To learn more about our background check program, please visit: https://hr.ucdavis.edu/departments/recruitment/ucd/selection/background-checks

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