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Medical Monitor Cro Jobs in Florida (NOW HIRING)

Research Assistant

Maitland, FL · On-site

$18 - $24.75/hr

... or CRO, Monitor{s), Auditors and any marketing groups hired by the Sponsor. * Utilize various psychiatric rating scales and maintaining interrater reliability with other clinicians at K2 Med. * ...

Clinical Research Coordinator

Lady Lake, FL · On-site

$21.25 - $28.25/hr

... or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor * Utilize various psychiatric rating scales and maintaining interrater reliability with other clinicians at K2 Medical ...

... and/or CRO, Monitor(s), Auditors and any central rating organizations hired by the Sponsor ... At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly ...

... and/or CRO, Monitor(s), Auditors and any central rating organizations hired by the Sponsor ... At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly ...

... and/or CRO, Monitor(s), Auditors and any central rating organizations hired by the Sponsor ... At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly ...

... and/or CRO, Monitor(s), Auditors and any central rating organizations hired by the Sponsor ... At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly ...

... and/or CRO, Monitor(s), Auditors and any central rating organizations hired by the Sponsor ... At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly ...

... monitoring visits with sponsor/(CRO) representatives. * Ensure the safety of study participants through appropriate training of staff and by working closely with Scientific and Medical Affairs.

... CRO industry * Experienced monitoring Oncology (I.e. Prostate Cancer, and Lung Cancer) and/or ... Health and wellbeing programmes including medical, dental, and vision coverage where applicable

Showing results 41-60

Medical Monitor Cro information

What is a medical monitor?

A Medical Monitor in clinical research, often employed by a Contract Research Organization (CRO), is a physician responsible for overseeing the safety and well-being of study participants during a clinical trial. They review clinical data, assess adverse events, and provide medical guidance throughout the trial to ensure compliance with regulatory requirements and good clinical practice. Medical Monitors also collaborate with investigators and sponsors to address medical questions and ensure that the study is conducted ethically and safely.

How does a medical monitor at a CRO typically interact with study sites and clinical teams during a trial?

A Medical Monitor at a CRO (Contract Research Organization) plays a central role in overseeing the medical aspects of clinical trials, collaborating closely with study site staff, investigators, and other clinical teams. They provide medical guidance, review safety data, and address any protocol deviations or adverse events as they arise. Regular communication—via calls, emails, and meetings—with site personnel ensures patient safety and data integrity throughout the study. This collaboration is essential for troubleshooting issues promptly and maintaining compliance with regulatory requirements.

What are the key skills and qualifications needed to thrive as a medical monitor in a CRO, and why are they important?

To thrive as a Medical Monitor in a CRO, you need an advanced medical degree (e.g., MD), clinical research experience, and a strong understanding of GCP and regulatory requirements. Familiarity with clinical trial management systems (CTMS), safety databases, and pharmacovigilance tools is typically required. Excellent analytical thinking, attention to detail, and effective communication are crucial soft skills for success in this role. These competencies ensure patient safety, data integrity, and smooth coordination between sponsors, sites, and study teams.

What is the difference between Medical Monitor Cro vs Medical Monitor?

AspectMedical Monitor CroMedical Monitor
CredentialsMedical degree, relevant clinical experience, often regulatory trainingMedical degree, clinical experience, regulatory knowledge
Work EnvironmentClinical trial sites, CRO offices, regulatory agenciesPharmaceutical companies, CROs, clinical research settings
Employer & IndustryContract Research Organizations (CROs), pharmaceutical industryPharmaceutical companies, CROs, biotech firms
Common Search/ComparisonMedical Monitor Cro vs Medical Monitor

The Medical Monitor Cro and Medical Monitor roles share similar credentials and work environments, often overlapping in clinical trial oversight within CROs and pharmaceutical companies. The main difference lies in their employment context: Medical Monitor Cro typically works within CROs on multiple client projects, while Medical Monitors may be employed directly by pharmaceutical companies. Both roles require medical expertise and regulatory knowledge, but their specific responsibilities and organizational settings differ slightly.

What job categories do people searching Medical Monitor Cro jobs in Florida look for?

The top searched job categories for Medical Monitor Cro jobs in Florida are:

Infographic showing various Medical Monitor Cro job openings in Florida as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution.

Clinical Research Coordinator

K2 Staffing LLC

Daytona Beach, FL • On-site

$23.25 - $31/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago


Key responsibilities

  • Manage clinical trial performance by ensuring conduct aligns with study protocols, federal regulations, and company guidelines.

  • Collect, record, and maintain source documentation and sponsor-required information related to clinical trials.

  • Perform clinical tasks such as vital signs, ECG, phlebotomy, and specimen handling, and educate patients about the study and clinical trials.


Job description

At K2 Medical Research, we are transforming healthcare by delivering tomorrow’s treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. Our culture is grounded in clinical excellence and a patient-first mission. We are seeking mission-driven individuals ready to play a meaningful role in bringing life-changing treatments to the patients who need them most.

K2 is seeking an experienced Clinical Research Coordinator to support our clinic out of Daytona Beach, FL

This position will manage clinical trial performance and ensure conduct is congruent to the philosophy and mission of K2 Medical Research. Promote good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federal regulations and K2 Medical Research guidelines (SOPs) for the enrollment and maintenance of subjects in clinical trials, and by collecting, recording, and maintaining source and sponsor documentation.

Primary Responsibilities:

  • Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator
  • Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate
  • Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator
  • Articulate all pertinent issues to the Pl or document by email/letter or during meetings
  • Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources
  • Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor
  • Utilize various psychiatric rating scales and maintaining interrater reliability with other clinicians at K2 Medical Research
  • Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging
  • Maintain timely K2 Medical Research source documentation as well as sponsor required information.
  • Dispense and maintain accurate records of study medication
  • Educate patients and family regarding their particular study and clinical drug trials in general.
  • Complete all monitor and sponsor queries in a timely manner
  • Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient's participation in study

Knowledge, Skills, and Abilities:

  • Outstanding verbal and written communication skills
  • Excellent interpersonal and customer services skills 
  • Strong time management and organizational skills 
  • In depth knowledge of industry regulations 
  • Proven ability to and foster mentoring relationships
  • Ability to create momentum and foster organizational change

Qualifications:

  • HS Diploma or GED Transcript required. Bachelor's degree strongly preferred.
  • Prior experience in a clinical environment preferred. Experience in clinical research and Parkinson's (neurodegenerative disease) is ideal.
  • Phlebotomy, LPN, RN, or other medical licensure or certification preferred.
  • Strong working knowledge of GCP and FDA guidelines.
  • Knowledge of medical terminology.
  • BLS Healthcare Provider desired.
  • Applicants that do not meet 100% of the above qualifications but who have a combination of related education and applicable experience may be considered upon approval.

Your growth and well-being are our priority. Our comprehensive benefits package for full-time employees includes medical, dental, and vision options, supplemental insurance plans, 401(k) with immediate employer match, generous paid time off, and paid holidays. Most notably, we support a healthy work-life balance through a four-day work week, consisting of 10-hour shifts from Monday through Thursday. Fridays are reserved only for critical business needs or administrative tasks; otherwise, they are your chance to kick-start your weekend.

Join the K2 Family: Where Compassion and Connection Lead the Way! At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff. 

We are an equal opportunity employer. We celebrate what makes you uniquely you and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital, or veteran statuses.

We value the differences among our team members and are committed to providing reasonable accommodations for qualified individuals with disabilities. If you require a reasonable accommodation to participate in the job application or interview process, please contact Talent@k2med.com. We are here to ensure you have the support and tools you need to shine.