Research Assistant

K2 Medical Research; Town of Florida (NY); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) with employer match

Paid time off and holidays

Four-day work week (Mon–Thu)

Job summary

K2 Medical Research is seeking a Clinical Research Assistant to support our Orlando (Maitland), FL clinic in the Phase I unit. You will promote good clinical practices under federal regulations, maintain source documentation, and assist in coordinating study activities with investigators and sponsors.

The role emphasizes patient screening, data collection, and communication among study staff, CROs, and sponsors.

Qualifications

• Excellent verbal and written communication skills required.
• Strong time management and organizational abilities.
• Experience in clinical environment a plus; licensed or certified personnel preferred.

Responsibilities

• Track and move candidates through screening.
• Read protocols and coordinate with Principal Investigator.
• Assist Site Director and Project Management on projects.
• Adhere to study protocol and communicate issues to CRO/Sponsor.
• Collect patient information and maintain source documentation.
• Dispense and maintain records of study medication.
• Educate patients about the study and trials.

Skills

Communication skills

Time management

Organizational skills

Interpersonal skills

Mentoring relationships

Education

HS Diploma or GED

Bachelor's degree

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 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 [e-mail]. We are here to ensure you have the support and tools you need to shine.