Clinical Research Coordinators (Future Openings • Connect Early)

Clinical Research Coordinators (Future Openings • Connect Early) jobs in United States

K2 Medical Research

• Clinical Trials

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

Preferred

• Bachelor's degree strongly preferred
• Bilingual in Spanish/English highly desired
• Strong working knowledge of GCP and FDA guidelines
• CCRC or CCRP certification (ACRP or SOCRA)
• Experience in specific therapeutic areas (e.g., Neurology, Oncology, Cardiology)

Benefits

• For full-time employees: medical, dental, and vision options
• For full-time employees: supplemental insurance plans
• For full-time employees: 401(k) with immediate employer match
• For full-time employees: generous paid time off
• For full-time employees: paid holidays
• For full-time employees: 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
• K2 Medical Research is a clinical research center that specializes in conducting clinical trials.
• Maitland, Florida, USA
• https://k2med.com
• Growth Stage
• Total Funding
• unknown
• Key Investors
• TPG
• 2024-06-17
• Private Equity
• Leadership Team
• Sean Stanton
• Founder
• Recent News
• FierceBiotech
• Chutes & Ladders—Legend poaches Novartis vet to boost commercial potential
• 2026-09-24
• PR Newswire
• K2 Medical Research Appoints Robert Massey as Chief Commercial Officer in Newly Created Role, Signaling Next Chapter of Growth
• 2026-09-15
• K2 Medical Research Opens Boston Area Site in Foxboro, MA - Expanding Access to Clinical Trials and Innovative Treatments
• 2026-06-02
• Company data provided by
• AI Tools

Qualifications

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

Required skills

• Clinical Research Site Experience, Clinical Practice (GCP), FDA Guidelines, CCRC Certification, CCRP Certification, Neurology, Oncology, Cardiology

Preferred skills

• Bachelor's degree strongly preferred, Bilingual in Spanish/English highly desired, Strong working knowledge of GCP and FDA guidelines, CCRC or CCRP certification (ACRP or SOCRA)

Experience

• Mid level