Jobs at K2 Medical Research

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.

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.

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.

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.

Leads regional physician engagement strategy across Florida clinics, managing Regional Navigators embedded in clinical practices. Builds provider relationships, strengthens clinical research referrals, oversees physician contracts and invoicing, analyzes engagement metrics, and presents performance insights to executives. Partners with clinical operations, marketing, and study teams to integrate research opportunities into routine care and improve physician participation.

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

Guides patients through clinical research opportunities by identifying potential candidates, prescreening, reviewing charts, matching patients to trials, coordinating appointments and documentation, and providing follow-up support. Maintains accurate records, protects patient confidentiality, supports informed decision-making, and follows FDA, ICH-GCP, ethical, and regulatory requirements while coordinating with clinic and research staff.

Supports clinical trial regulatory activities, including IRB and sponsor submissions, regulatory file maintenance, safety and deviation reporting, informed consent updates, delegation logs, monitoring visits, study start-up, amendments, closeout, and archiving. Collaborates with clinical operations, sponsors, monitors, finance, and IRBs while ensuring audit readiness, timely document distribution, and compliance with protocol and regulatory requirements.

Coordinates clinical trial activities in a mobile research clinic, including protocol adherence, patient interviews, clinical assessments, phlebotomy, ECGs, specimen handling, medication dispensing, source documentation, patient education, and communication with sponsors, CROs, monitors, clinicians, and families. Maintains regulatory and study records, resolves queries, supports monitoring activities, and provides referrals at study completion.

Supports clinical trial regulatory activities, including IRB and sponsor submissions, regulatory file maintenance, protocol deviation and safety reporting, informed consent updates, delegation logs, monitoring visits, study closeout, and archiving. Coordinates with clinical operations, sponsors, monitors, finance, and IRBs while maintaining audit-ready documentation and tracking submission status.

The Quality Control Associate performs source-data and Investigator Site File reviews to verify protocol eligibility, regulatory compliance, training documentation, and adherence to SOPs. The role creates queries, tracks compliance trends and metrics, reports quality issues, supports quality management resolutions, and provides training to clinical research staff. This hybrid position requires weekly clinic support in The Villages, Florida, and experience with clinical research and patient care.

Supports Corporate Counsel by drafting, reviewing, formatting, routing, and tracking clinical research and corporate agreements. Maintains contract templates, playbooks, standard operating procedures, legal documentation, and contract lifecycle systems. Collaborates with clinical operations, finance, compliance, business development, vendors, sponsors, CROs, and research sites. Assists with compliance initiatives, basic legal research, risk identification, and scalable legal process improvements.

Supports clinical investigations by ensuring protocol compliance, Good Clinical Practice, IRB oversight, accurate documentation, data integrity, and proper handling of investigational agents. Provides medical care and treatment to study participants, maintains licensure and qualifications, oversees study procedures, and collaborates with investigators and research staff. Requires Florida licensure as a PA, NP, or ARNP and at least two years of clinical experience.

Provides front-desk reception and office management support in a clinical research clinic. Responsibilities include greeting visitors, answering and directing calls, managing mail and deliveries, scheduling meetings, maintaining reception supplies and records, controlling visitor access, updating databases, and completing clerical tasks. The role requires bilingual English and Spanish communication, multitasking, attention to detail, and the ability to work a four-day Monday–Thursday schedule in a fast-paced clinical environment.

Guides patients through clinical research opportunities by identifying eligible participants, conducting prescreening and chart reviews, matching patients to trials, coordinating appointments and documentation, and providing follow-up support. Maintains accurate records, protects patient confidentiality, follows FDA and ICH-GCP requirements, and collaborates with clinic and research staff. The role also provides patient education, resource referrals, and compassionate communication throughout the research process.