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  3. Clinical Research Coordinator
KS

Clinical Research Coordinator

K2 Staffing LLC·Maitland, Florida

Full Time·On Site·2-5 yrs·Posted 26 days ago
Practice for this role

About the role

Manage clinical trial performance and ensure adherence to study protocols and federal regulations. Perform clinical tasks including phlebotomy and ECGs while maintaining accurate source documentation and patient communication.

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 Maitland, 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

  • Bilingual in Spanish/English highly desired.
  • 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.

Requirements

Requires a high school diploma or GED, with a bachelor's degree and clinical research experience strongly preferred. Proficiency in GCP/FDA guidelines and medical licensure (LPN, RN, or Phlebotomy) is highly desired.

  • high school
  • bachelor degree
  • professional certificate
  • Time Management
  • Organizational Skills
  • Interpersonal Communication
  • Phlebotomy
  • Medical Terminology
  • Patient Education
  • Source Documentation
  • Vital Signs Monitoring
  • Patient Recruitment
  • Clinical Research Coordination
  • FDA Regulations
  • Clinical Trial Management
  • ECG
  • GCP Guidelines
  • Psychiatric Rating Scales
  • Spanish Bilingualism

Benefits

  • Dental Insurance
  • Paid Holidays
  • Paid Time Off
  • Vision Insurance
  • Medical Insurance
  • Supplemental Insurance Plans
  • Four-Day Work Week
  • 401(k) With Immediate Employer Match

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Location
Maitland, Florida
Posted
Jul 2, 2026
Application
Employer website
KS

Hiring organization

K2 Staffing LLC

K2 Staffing has been constructed on one of the most solid foundations in the industry, with roughly 40 years of combined business and recruiting knowledge. Through our vast experience, we understand locating and attracting the right talent can be comparable to ascending K2 -...

Salary listed on 1 job
IndustryStaffing and Recruiting
TypePrivately Held
Size2-10 employees
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Market context

Florida clinical research roles stay competitive

Clinical Research Coordinator openings in Florida often draw candidates with hands-on trial coordination and strong compliance skills, especially in settings running active studies. This role is competitive because employers look for experience with regulatory documentation, medical record accuracy, and familiarity with clinical trial procedures. Review the AI-summarized requirements and benefits here to save research time, then tailor your application to show direct coordinator or research assistant experience.

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