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K2 Staffing LLC logo

Research Assistant

K2 Staffing LLC·Maitland, Florida

Full TimeOn Site0-2 yrsPosted 6 days ago
Practice for this role

Research Assistant

How this role compares

Computed from live listings

  • 18 similar openings in the Maitland area

About the role

The Clinical Research Assistant supports clinical trial performance by managing patient screening, maintaining accurate source documentation, and ensuring strict adherence to study protocols. They also perform clinical tasks such as vital signs, phlebotomy, and ECG while facilitating communication between patients, investigators, and sponsors.

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 Clinical Research Assistants to support our clinic out of Orlando (Maitland), FL in the Phase I unit.

The Clinical Research Assistant will support clinical trial performance and conduct 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

  • Track and move candidates through screening efficiently. Aiding the coordinators and keeping subjects from falling through the cracks.
  • Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator.
  • Assist the Site Director and Project Management team on projects as needed.
  • 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 Med.
  • 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 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 is ideal.
  • LPN, RN, or other medical licensure or certification preferred.
  • Applicants that don't meet 100% of the above qualifications but who have a combination of related education, applicable experience, demonstrated capability, and a genuine passion for success in this position may also be consider.

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

Candidates must have at least a high school diploma or GED, with a bachelor's degree strongly preferred. Prior experience in a clinical or research environment and relevant medical licensure such as LPN or RN are considered highly desirable.

  • high school
  • bachelor degree
  • professional certificate
  • Phlebotomy
  • Organizational skills
  • Communication skills
  • Customer service
  • ECG
  • Time management
  • Patient education
  • Regulatory compliance
  • Vital signs monitoring
  • Clinical research
  • Protocol adherence
  • Patient screening
  • Psychiatric rating scales
  • Specimen packaging
  • Source documentation

Benefits

  • Dental insurance
  • Vision insurance
  • Medical insurance
  • Paid holidays
  • Generous paid time off
  • Supplemental insurance plans
  • 401(k) with immediate employer match

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
0-2 yrs
Location
Maitland, Florida
Posted
Sep 1, 2026
Application
Employer website
K2 Staffing LLC logo

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 -...

IndustryStaffing and Recruiting
TypePrivately Held
Size2-10 employees
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Market context

Florida research assistant roles favor clinical experience

In Florida, research assistant openings in healthcare settings often draw candidates with clinical or clinical research experience, and employers may prefer applicants with a bachelor’s degree and licensure such as LPN or RN. This role is competitive because it blends patient-facing familiarity with research support tasks, while the job requirements and benefits on this platform are AI-summarized from the original posting to save you research time. If you are applying, highlight any clinical workflow, data collection, or protocol support experience and confirm your diploma, degree, or licensure details are easy to verify.

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