Research Assistants

Automatic Data Processing, Inc.; Florida; On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Medical benefits

Dental & Vision

401(k) with match

Paid time off

Paid holidays

Four-day work week

Friday flexibility

Job summary

K2 Medical Research in Florida seeks Clinical Research Assistants for the Phase I unit in The Villages, FL. You will support trial conduct, maintain regulatory source docs, and assist the Site Director and PM team on studies.

Qualified applicants have a HS diploma or GED (Bachelor's preferred), clinical experience, and relevant licensure. Benefits include medical/dental/vision, 401(k) with match, paid time off, and a four‑day work week (Mon–Thu).

Qualifications

• HS Diploma or GED required; Bachelor's degree strongly preferred.
• Experience in a clinical environment preferred; clinical research ideal.
• LPN, RN, or other medical licensure/certification preferred.
• Candidates not meeting 100% of qualifications may be considered with related education/experience.

Responsibilities

• Track and move candidates through screening with coordinators.
• Read protocols and coordinate with Principal Investigator.
• Assist Site Director and Project Management on projects.
• Adhere to study protocol; obtain exemptions when needed.
• Communicate issues to CRO/Sponsor and study team.
• Collect initial psychiatric/medical information from patients.
• Maintain source documentation and sponsor data.

Skills

Verbal and written communication

Interpersonal skills

Time management

Regulatory knowledge

Mentoring and change facilitation

Education

HS Diploma or GED

Bachelor's degree preferred

LPN/RN licensure preferred

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Research Assistants

Full Time Technical Lady Lake, FL, US

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 The Villages, 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.