Top 2762 Crc Jobs | SimplyHired

Clinical Research Coordinator
START Center for Cancer Research —Grand Rapids, MI
- Monday to Friday
- Mid-level
- High school diploma or GED
- Travel
- Health savings account
- Paid holidays
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9d
Clinical Research Coordinator
Burke Rehabilitation Hospital —White Plains, NY
- $70,000 a year
- Full-time
- Hospital
- HIPAA
- Inpatient
9d
Clinical Research Coordinator (CRC)
United Theranostics —Princeton, NJ
- $70,000 - $98,000 a year
- Full-time
- 5 years
- Mid-level
- 3 years
- Health insurance
- Dental insurance
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Clinical Research Coordinator
Segal Institute for Clinical Research —North Miami, FL
- Full-time
- Bilingual
- Vital signs
- Mid-level
- Health insurance
- Dental insurance
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2d
Clinical Scientist / Rater Trainer - CNS
Cognitive Research Corporation —Remote
- Remote
- Microsoft Outlook
- Doctoral degree
- Travel
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3d
Senior Clinical Research Associate - CNS
Cognitive Research Corporation —Remote
- Remote
- 5 years
- English
- Bachelor's degree
Quick Apply
11d
FEDERAL LEGAL TRANSCRIBER (Remote Contractor)
CRC Salomon —Remote
- From $600 a week
- Part-time
- Microsoft Word
- English
- Research
- Flexible schedule
Quick Apply
Telehealth Medical Coder – CRC Required - Remote
CareTalk Health —Remote
- $30 an hour
- Full-time
- Remote
- Background check
- Clinic experience
- Mid-level
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Senior Clinical Trial Manager
Aveera Medical —Remote
- $125,000 - $175,000 a year
- Full-time
- Remote
- 7 years
- Organizational skills
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator I - VESPER
Henry M. Jackson Foundation —Washington, DC
- $52,800 - $57,164 a year
- Full-time
- Hybrid work
- Entry level
- Health insurance
- Dental insurance
Assistant CRC
University of California San Francisco —San Francisco, CA
- Full-time
- HIPAA
- Windows
- High school diploma or GED
HCC Medical Coder
vArida-Tech —Remote
- $10 - $11 an hour
- Contract
- Remote
- HIPAA
- Mid-level
Quick Apply
Research Assistant
CenExel IResearch LLC —Decatur, GA
- $20 - $21 an hour
- Psychiatry
- Office
- Neurology
- Health insurance
- Dental insurance
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Clinical Research Associate
Georgetown University —Washington, DC
- $47,586.00 - $87,558.13 a year
- Full-time
- Patient monitoring
- 5 years
- Mid-level
- Disability insurance
- Health insurance
Clinical Research Coordinator (CRC) I
Pharmaron —Baltimore, MD
- Full-time
- 1 year
- Associate's degree
- Entry level
Quick Apply
Clinical Research Coordinator
Foundation for Atlanta Veterans Education and Research, Inc. —Decatur, GA
- $40,000 - $80,000 a year
- Full-time
- Medication administration
- Patient monitoring
- Writing skills
Quick Apply
8d
Risk Adjustment Analyst
PCC MEDICAL HOLDINGS LLC —North Palm Beach, FL
- $65,000 - $75,000 a year
- Full-time
- Remote
- Mid-level
- Analysis skills
- 2 years
Quick Apply
Medicare Quality & Risk Adjustment Program Lead - Aspire Health
Montage Health —Remote
- $128,876 a year
- Full-time
- Nursing
- RN License
- Analysis skills
CLINICAL RESEARCH COORDINATOR I
University of Alabama at Birmingham —Birmingham, AL
- $43,890 - $71,320 a year
- Day shift
- High school diploma or GED
- University
- Psychology
4d
CRC OHN
University of California San Francisco —San Francisco, CA
- Full-time
- Writing skills
- HIPAA
- Mid-level

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Clinical Research Coordinator

START Center for Cancer Research -
Grand Rapids, MI

Quick Apply

Job Details

9 days ago

Benefits

Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
401(k) matching

Qualifications

Computer operation
Medical software
Regulatory compliance
High school diploma or GED
Oncology research
Patient interaction
Productivity software
Clinical quality assurance standards
Oncology

Full Job Description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe.

We are currently hiring a Clinical Research Coordinator. The Clinical Research Coordinator (CRC) will work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The Clinical Research Coordinator will be assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial. Also, this role is responsible for implementation as well as completion of protocol specific requirements, providing accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements.

Work Schedule: Monday-Friday 8:00am-5:00pm

Location: START Midwest - 800 Foremost Dr SE Grand Rapids, Michigan 49546

Essential Responsibilities:

Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol.
Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.
Create/review forms created or revised for assigned trials to assure protocol compliance.
Maintain files using standardized study document labeling and filing procedures.
Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.
Maintain an up-to-date contact list.
Assist with patient screening and determination of eligibility.
Facilitate the informed consent process ensuring that consent is appropriately completed.
Prepare and manage source documents according to standard operating procedures.
Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.
Assist data coordinator team with case report form completion and query resolution.
Work with the Principal Investigator to complete and submit Serious Adverse Event reports.
Perform protocol specific closeout related activities in conjunction with the data coordinator.
Provide documentation for all deviations whether related to the protocol or a SOP.
Ensure that all team members involved understand and adhere to assigned protocols.

Required Education and Experience:

High School Diploma or GED.
2 years of clinical research experience.
Basic understanding of oncology clinical trials, particularly Phase 1 studies.
Strong attention to detail and accuracy in data collection and documentation.
Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
Excellent organizational and time-management skills.
Strong communication skills, both written and verbal.
Ability to interact professionally with patients, study staff, and external stakeholders.
Working knowledge of GCP and regulatory requirements.
Proficient in Microsoft Office Suite and clinical trial management software.

Preferred Education and Experience:

Experience working in an oncology setting.

Physical & Travel Requirements:

Sitting: Must be able to sit for extended periods of time.
Prolonged use of computer, keyboard, and mouse.

Best-in-Class Benefits and Perks

We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:

401(k) retirement savings plan with employer match

Eligibility for an annual performance bonus, based on role and company results

Generous paid time off and paid holidays

Comprehensive medical, dental, and vision coverage and optional insurance options

Company p‑aid life and disability insurance for added financial protection

Employee Assistance Program (EAP) providing confidential, no ‑cost support for you and your family from day one

Flexible FSA and HSA plans to support your financial wellness

Commitment to a supportive environment that values balance, wellbeing, and flexibility

We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – one of the most effective cancer drugs in medical history.

Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Work Location: In person

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