Clinical Research Coordinators (Future Openings • Connect Early)

ADP, Inc.; Florida; On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

4-day work week

Competitive benefits

401(k) with employer match

Paid time off

Job summary

K2 Medical Research is seeking Clinical Research Coordinators to support our Orlando (Maitland), FL clinic as part of evergreen opportunities. We prioritize patient-centered, compliant conduct of multi-phasic trials across therapeutic areas and seek mission-driven professionals to join our team.

As a fast-growing CRO, you will ensure quality data collection, follow GCP guidelines, and collaborate with investigators, sponsors, and site staff to advance clinical trials.

Qualifications

• Direct experience working at a clinical research site.
• Bachelor’s degree strongly preferred; HS Diploma or GED required.

Responsibilities

• Understand assigned studies by reading protocols and coordinating with Principal Investigator.
• Adhere to study protocol and obtain exemptions when appropriate.
• Communicate protocol issues to CRO/Sponsor and study staff.
• Collect initial psychiatric and medical information by interviewing patients.
• Maintain source documentation and sponsor data.
• Dispense and manage study medication records.

Skills

Clinical research experience

Communication skills

Interpersonal skills

Mentoring relationships

Education

HS Diploma or GED

Bachelor’s degree 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.

Clinical Research Coordinators (Future Openings Connect Early)

Full Time Professional Maitland, FL, US

3 days ago Requisition ID: 1223

This is anevergreen requisition, meaning we don't have an immediate opening, but we're actively seeking talented professionals for upcoming opportunities. By applying, your information will be reviewed and considered for future roles as they become available. If you're interested in a future with K2 Medical Research, we encourage you to apply!

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.

K2is seeking experienced Clinical Research Coordinatorsto support our clinic out of Orlando (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.

Qualifications:

• Required:
  • Proven direct experience working at a clinical research site.
  • HS Diploma or GED Transcript required. Bachelor's degree strongly preferred.
• Preferred:
  • Bilingual in Spanish/English highly desired.
  • Strong working knowledge of GCP and FDA guidelines.
  • CCRC or CCRP certification (ACRP or SOCRA) AND Experience in specific therapeutic areas (e.g., Neurology, Oncology, Cardiology)

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
• Proven ability to and foster mentoring relationships
• Ability to create momentum and foster organizational change

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.