Jobs at K2 Medical Research

Recruits and prescreens patients for multiple clinical trials, identifies potential candidates, schedules screening visits, maintains recruitment trackers and patient databases, follows up with patients, and ensures familiarity with study protocols. The role requires strong communication, organization, multitasking, attention to detail, and proficiency with Microsoft Office. Bilingual English-Spanish skills and experience in healthcare, patient recruitment, or clinical research are preferred.

Recruits and prescreens patients for clinical research studies, identifies potential participants, schedules screening visits, maintains recruitment trackers and patient databases, and follows up with patients. The role requires understanding study protocols, completing training, coordinating with clinical teams, and communicating effectively with a diverse patient population. It is remote but requires travel to Tampa, Florida.

Supports clinical trial operations by screening and communicating with patients, collecting medical information, performing clinical tasks such as vital signs, ECGs, phlebotomy, and specimen packaging, maintaining study documentation and medication records, addressing sponsor queries, adhering to protocols and regulations, and educating patients and families about clinical studies.

Administers and interprets cognitive, diagnostic, clinical, and psychometric assessments for pharmaceutical clinical trials involving neurological and mental health conditions. Conducts caregiver interviews, telephone screens, and protocol-specific ratings; maintains accurate study documentation, responds to queries, supports subject safety, and communicates with investigators, sponsors, CROs, and study teams. Supervises study lead activities and coordinators while ensuring compliance with protocols, Good Clinical Practice, company policies, and applicable regulations.

Coordinate clinical trials by reviewing protocols, enrolling and educating patients, collecting medical data, performing clinical procedures, maintaining source and sponsor documentation, dispensing study medication, addressing queries, and communicating with investigators, sponsors, CROs, monitors, and auditors. Ensure compliance with protocols, Good Clinical Practice, FDA guidelines, and organizational SOPs while supporting patient safety and study quality.

Supports clinical trials by screening and tracking candidates, reviewing protocols, collecting medical and psychiatric information, performing clinical tasks such as vital signs, ECGs, phlebotomy, and specimen packaging, maintaining source and sponsor documentation, dispensing study medication, communicating with sponsors and CROs, resolving queries, and educating patients and families.

Manage site-level regulatory operations for concurrent clinical trials, including IRB submissions, protocol amendments, continuing reviews, safety reports, informed consent forms, DOA logs, regulatory binders, and eReg documentation. Drive study start-up workflows through site initiation and activation, track timelines, coordinate with sponsors, CROs, IRBs, and internal teams, and support GCP, FDA, and sponsor compliance during audits and monitoring.

Maintain audit-ready regulatory files for clinical trials, including eRegulatory platforms, essential documents, IRB approvals, protocol training, regulatory submissions, and monitoring closeout updates. Coordinate with clinical operations, sponsors, and regulatory teams; support quality reviews, onboarding, document processing, and network site coverage. The role is hybrid in Orlando, Florida, requiring strong organization, communication, technology proficiency, confidentiality, and attention to detail.

Leads clinical research coordination and project management activities, supervises Project Managers, trains staff, supports site operations, ensures protocol and regulatory compliance, coordinates with sponsors and investigators, collects patient data, performs clinical procedures, manages study medication and documentation, resolves queries, and educates patients and families.

Provides part-time PRN clinical support for clinical trials, including IV access and maintenance, investigational product administration, patient monitoring, infusion reaction assessment, and trial procedures such as lumbar punctures, lab collections, and EKGs. Requires a valid Florida RN, LPN, or paramedic license, clinical experience, attention to detail, professional communication, and adherence to Good Clinical Practice.

Supports Phase I clinical trials by screening and tracking candidates, reviewing protocols, collecting medical and psychiatric information, performing clinical tasks such as vital signs, ECGs, phlebotomy, and specimen packaging, maintaining source and sponsor documentation, dispensing study medication, resolving queries, communicating with sponsors and CROs, educating patients and families, and providing referrals after study participation.

Administer, score, and interpret cognitive, diagnostic, clinical, and psychometric assessments for pharmaceutical clinical trials involving neurological and mental health conditions. Conduct caregiver interviews, telephone screens, and eligibility evaluations while following study protocols, FDA requirements, Good Clinical Practice, and company SOPs. Maintain accurate documentation, address queries, communicate rating issues, support participant safety, and supervise study lead and coordinator scheduling duties.

Provides medical oversight for clinical research patients and study teams. Reviews trial eligibility, conducts patient assessments and physical examinations, interprets laboratory results, EKGs, and safety data, monitors adverse events, ensures accurate documentation and protocol compliance, and collaborates with physicians, nurses, and research personnel. The role is onsite and full-time, with training provided and occasional travel for study-related meetings.

Performs quality control reviews of clinical research source documents, investigator site files, eligibility records, training documentation, and regulatory compliance. Coordinates with Quality Management and clinical sites to resolve issues, create queries, track compliance trends, report quality concerns, and provide staff training. The role requires hybrid clinic support in Florida, independent work, strong organizational and communication skills, and knowledge of clinical research regulations and SOPs.

Manage clinical trial activities, including protocol adherence, patient interviews, clinical assessments, documentation, medication dispensing, sponsor communication, query resolution, and patient education. Perform vital signs, ECGs, phlebotomy, specimen handling, and psychiatric rating scales while maintaining regulatory and source records. Coordinate with investigators, sponsors, CROs, monitors, auditors, patients, and families throughout study participation.

Administer and score cognitive, diagnostic, and clinical assessments for pharmaceutical clinical trials involving neurological and mental health conditions. Conduct caregiver interviews, telephone screens, and protocol-specific psychometric testing; evaluate eligibility, maintain accurate source documentation, address queries, and communicate with investigators, sponsors, CROs, and study staff. The role also supports participant safety, regulatory and GCP compliance, study scheduling, coordinator supervision, and consistent assessment practices.

Coordinates clinical trials by reviewing protocols, enrolling and educating patients, collecting medical data, performing clinical procedures, maintaining source and sponsor documentation, managing study medication, resolving queries, and communicating with investigators, sponsors, CROs, monitors, and auditors. Ensures compliance with protocols, Good Clinical Practice, FDA regulations, and organizational SOPs while supporting patient care and study quality.

Supports clinical trial execution by screening and tracking candidates, reviewing protocols, collecting medical and psychiatric information, performing clinical procedures, maintaining source and sponsor documentation, dispensing study medication, resolving queries, communicating with sponsors and clinical teams, and educating patients and families. Requires strong organization, communication, regulatory knowledge, and adherence to study protocols and good clinical practices.

Recruits and prescreens patients for multiple clinical studies, identifies potentially eligible participants, schedules screening visits, maintains recruitment trackers and patient databases, and follows up with patients. The role requires understanding study protocols, completing training, coordinating with clinical teams, and communicating effectively with a diverse patient population in English and Spanish.

Provides medical oversight for clinical research teams and trial patients. Reviews eligibility, performs patient assessments and physical examinations, interprets laboratory, EKG, and diagnostic results, monitors safety and adverse events, ensures accurate documentation and GCP compliance, and collaborates with physicians, nurses, and study personnel to execute clinical protocols.