Research Assistant
K2 Medical Research
- Location
- Maitland, FL
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 13
- 9 days ago
Career path
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About the company
K2 Medical Research
Research · 11 to 50 employees
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.
What you'll do
- 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.
What you need
- 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.
- Education: a high school diploma or a bachelor's degree
Key skills
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Perks
- medical
- dental
- vision options
- supplemental insurance plans
- 401(k) with immediate employer match
- generous paid time off
- paid holidays
- four-day work week
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