Rodeo
ResourcesPartnersSign in

Johns Hopkins All Children's Hospital

Clinical Research Coordinator II

Clacton-on-Sea
$27 – $45/hr
Posted about 9 hours ago
Sign up to applySee more jobs like this

How your CV stacks up

1Upload CV
2Analyse CV
3Improve CV

Upload your CV to see how well it fits this job role

?%

Clinical Research Coordinator II (CRC II) – Oncology Research Program

Location: St. Petersburg, FL

Schedule: Full-Time | Day Shift | On-Site (5 Days/Week)

This position is grant-funded for a period of five years and is therefore considered temporary in nature. While the role is expected to continue for the duration of the grant, ongoing employment is contingent upon continued funding.


Position Summary

We are seeking an experienced Clinical Research Coordinator II to support oncology clinical trials within our Pediatric Oncology Research Program. This role is responsible for coordinating complex clinical studies, ensuring regulatory compliance, supporting patient enrollment and follow-up, and collaborating with investigators, research staff, sponsors, and study participants.

The ideal candidate will have prior clinical research experience, strong organizational skills, and the ability to manage multiple studies while maintaining compliance with GCP, FDA regulations, and institutional policies.


Key Responsibilities

  • Coordinate and manage multiple oncology clinical trials from start-up through closeout.
  • Screen, recruit, consent, and follow study participants.
  • Review study protocols and ensure compliance with research requirements.
  • Prepare and submit regulatory documents to IRBs and sponsors.
  • Maintain study records, source documentation, and regulatory files.
  • Report adverse events, serious adverse events, and protocol deviations.
  • Complete data entry and manage study information within electronic systems.
  • Collaborate with investigators, research nurses, sponsors, and other study team members.

Reasons to use Rodeo

I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.

Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.

Start with a chat, not a search bar

Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.

P

Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

See breakdown
Save jobNot relevant
View details

It searches the market for you

Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.

Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

See breakdown
Strong

Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

See breakdown
Strong

Only hits

No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.


Required Qualifications

  • Bachelor’s degree in a health science, biological science, nursing, public health, or related field.
  • Clinical research coordination experience, preferably with interventional clinical trials.
  • Knowledge of Good Clinical Practice (GCP), FDA regulations, informed consent, and IRB processes.
  • Strong organizational, communication, and problem-solving skills.
  • Ability to manage multiple priorities in a fast-paced environment.

Preferred Qualifications

  • Oncology or pediatric oncology research experience.
  • Experience with regulatory submissions and compliance.
  • Clinical research certification (CCRC, CCRP, or equivalent).
  • Experience using EPIC, OnCore, REDCap, Rave, Veeva Vault, or similar research systems.

Why Join Us?

Join a collaborative research team dedicated to advancing pediatric oncology care through innovative clinical trials. This is an opportunity to make a meaningful impact on patients and families while contributing to groundbreaking cancer research.


Please Note: This is an on-site position in St. Petersburg, Florida. Candidates must be able to work on campus five days per week and reside locally or be willing to relocate.

Get help with your application

Your very own career expert that helps elevate your application to the next level.

Get help applying for this job

Salary Range: Minimum 27.85/hour - Maximum 44.57/hour. Compensation will be commensurate with equity and experience for roles of similar scope and responsibility. In cases where the range is displayed as a $0 amount, salary discussions will occur during candidate screening calls, before any subsequent compensation discussion is held between the candidate and any hiring authority.

The Hospital reserves the right to modify employee schedules as needed.

We are committed to creating a welcoming and inclusive environment, where we embrace and celebrate our differences, where all employees feel valued, contribute to our mission of serving the community, and engage in equitable healthcare delivery and workforce practices.

Johns Hopkins Health System and its affiliates are an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity and expression, age, national origin, mental or physical disability, genetic information, veteran status, or any other status protected by federal, state, or local law.

Johns Hopkins Health System and its affiliates are drug-free workplace employers.

Trusted by 25,000+ job seekers

“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”

Jessica, London

Get help applying for this job

Skills

Clinical Research Coordination
Regulatory Compliance
Patient Enrollment
Data Entry
Organizational Skills
Communication Skills
Problem-Solving Skills
Good Clinical Practice
FDA Regulations
Informed Consent
IRB Processes
Oncology Research
Pediatric Oncology
Regulatory Submissions
Clinical Research Certification
Research Systems

Location

Clacton-on-Sea, England, United Kingdom

Sign up to applySee more jobs like this