Top 3 Senior clinical research coordinator Jobs in Orlando Fl

Clinical Research Site Development Manager/Senior CRC
CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC. —Winter Park, FL
- Background check
- Management
- Mid-level
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9d
Sr. Lead Clinical Research Coordinator
Cardiovascular Associates of America —Lake Nona, FL
- Full-time
- Clinic experience
- Clinic
- Bachelor's degree
- Flexible schedule
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5d

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Sr. Lead Clinical Research Coordinator
Cardiovascular Associates of America —Lake Nona, FL
Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research). Clinical research certification (e.g., CCRP) is a plus.
Quick Apply
5d
Clinical Research Site Development Manager/Senior CRC
CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC. —Winter Park, FL
Coordinate qualification calls and Site Qualification Visits. When applying, please highlight your experience securing studies, developing sponsor/CRO…
Quick Apply
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Senior Clinical Research Coordinator
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Implements the requirements of clinical research protocols in compliance with local, state, institutional, Federal (FDA, DHHS) and sponsor requirements.
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Bachelor’s degree or equivalent experience in medical/science field. Reviews study protocols in order to write consent/assent documents and develop the initial…
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Clinical Research Site Development Manager/Senior CRC

CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC. -
Winter Park, FL

Quick Apply

Job Details

9 days ago

Qualifications

Patient recruitment
Clinical trial site selection

Full Job Description

Clinical Research Site Development Manager / Senior CRC

Sterling Clinical Research – Central Florida

Sterling Clinical Research is seeking an experienced Clinical Research Site Development Manager / Senior CRC to help grow and manage our expanding clinical research operation.

KEY REQUIREMENT: EXPERIENCE SECURING CLINICAL TRIALS

This is not a traditional CRC position.

We are specifically looking for someone with experience identifying, pursuing, and securing clinical trials from sponsors, pharmaceutical/biotech companies, and CROs.

The ideal candidate understands the full clinical research lifecycle—from study acquisition and feasibility through budget negotiation, site start-up, enrollment, study execution, and closeout.

You Will Have Dedicated Support

You will not be expected to do everything alone.

This position will have a dedicated Assistant CRC to assist with patient scheduling, study coordination, documentation, regulatory tasks, and other day-to-day research activities.

This allows you to focus more heavily on higher-level responsibilities, including bringing new trials to the site, developing sponsor/CRO relationships, negotiating budgets, managing study start-up, and overseeing successful trial execution.

Key Responsibilities

Identify and pursue new clinical trial opportunities

Develop and maintain relationships with sponsors and CROs

Complete feasibility questionnaires and site-selection submissions

Present our site capabilities to potential sponsors

Coordinate qualification calls and Site Qualification Visits

Negotiate study budgets, start-up fees, and other site costs

Assist with Clinical Trial Agreement (CTA) negotiations

Manage regulatory and site start-up activities

Oversee study activation, enrollment, monitoring, and closeout

Coordinate with investigators, sponsors, CROs, and research staff

Supervise and work closely with the dedicated Assistant CRC

Ensure compliance with GCP, FDA, IRB, and protocol requirements

What We’re Looking For

3+ years of clinical research experience preferred

Proven experience obtaining or helping secure clinical trials for a research site

Experience working directly with sponsors and CROs

Experience with feasibility questionnaires and site selection

Experience with study start-up and regulatory processes

Experience negotiating clinical trial budgets

Strong knowledge of GCP and clinical research regulations

Highly organized, proactive, and comfortable taking ownership

Experience in orthopedics, pain management, spine, neuroscience, or medical device trials is a plus

Why Sterling Clinical Research?

Sterling Clinical Research has something many growing research sites spend years trying to develop:

Patients. Physicians. Facilities. Infrastructure.

Our research operation has access to:

75,000+ patients

13 affiliated medical clinics

Board-certified specialists

Orthopedic, Neurosurgery & Pain Management capabilities

In-house MRI

C-Arm procedure suites and X-ray capabilities

Established patient referral and recruitment infrastructure

Dedicated Assistant CRC support

Our goal is to continue building Sterling Clinical Research into a premier clinical research site in Central Florida.

We already have the infrastructure and patient population. We need an experienced research professional who knows how to turn those capabilities into clinical trial opportunities.

We Especially Want to Hear From You If…

You can confidently say:

“I know how to get clinical trials into a research site.”

When applying, please highlight your experience securing studies, developing sponsor/CRO relationships, negotiating budgets, and launching clinical trials.

Background Screening (Florida): This position requires Level 2 screening through the Florida Care Provider Background Screening Clearinghouse. Learn more: https://info.flclearinghouse.com

Quick Apply

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Clinical Research Site Development Manager/Senior CRC

Sr. Lead Clinical Research Coordinator

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