Jobs at DM Clinical Research

Prepare, compound, dispense, store, and document investigational products per sponsor protocols; manage IP accountability and temperature logs; perform data audits; support study start-up, onboarding, and regulatory document maintenance; train staff and liaise with investigators and sponsors.

Manage and oversee conduct of clinical trials at assigned investigative sites to ensure protocol compliance, participant enrollment, data quality, safety reporting, site training, regulatory adherence (FDA/ICH-GCP), and timely study execution from first patient first visit through close-out.

Manage and ensure quality conduct of clinical trials at assigned investigative sites from first patient in to close-out. Oversee protocol adherence, training (ICH-GCP/IATA/EDC/IVRS), site readiness, informed consent, data quality (ALCOA-C), safety reporting, enrollment targets, regulatory compliance, and cross-functional coordination.

Dispense and manage investigational products per protocol, maintain IP accountability and storage, ensure blinding compliance, perform clinical data audits, support site startup and onboarding, develop SOPs and workflows, and coordinate with investigators, sponsors, and study teams.

Manage clinical trial activities at assigned investigative sites ensuring protocol, FDA, and ICH-GCP compliance. Oversee site training, visit preparedness, source document review, safety and adverse event reporting, data quality, enrollment targets, and study closeout. Coordinate cross-functional teams and support site staff and leadership.

Coordinate and document clinical trial activities at investigative sites to ensure protocol compliance, data quality, and enrollment targets. Complete required trainings/certifications, perform subject visits, manage lab procedures and data entry, liaise with sponsors/CROs, support recruitment/consent, and follow site management directions to meet study and regulatory requirements.

Dispense and manage investigational products per sponsor protocols, maintain IP accountability and storage, support study startup and regulatory documentation, train and supervise team members, perform data audits, and liaise with investigators and sponsors to ensure protocol compliance.

Manage clinical research site operations to ensure protocol compliance, data quality, subject enrollment and retention. Supervise site staff, complete required training (ICH-GCP, IATA), ensure visit preparedness, oversee study conduct from first patient first visit to closeout, and communicate with sponsors, IRBs, and study teams.

Manage review and negotiation of CRO/sponsor budgets and contract amendments, maintain financial KPIs and budget decision logs, oversee contract execution and upload to contract system, build stakeholder and vendor relationships, ensure timely and accurate internal reporting, and support continuous improvement of budgeting and contracting processes.

Manage SocialPilot and Google Business Profiles for multi-site organic social, local content collection, event recaps, content calendars, approvals, and reporting. Align organic content with performance marketing, coordinate with sites and creative teams, use AI and video tools to create localized patient-education and trust-building content while ensuring regulatory and approval compliance.

Entry-level role supporting finance and clinical systems: configure stipends and study setups in CRIO, verify monthly invoices, validate cross-system data, manage Clincard and patient funds, maintain operational trackers, respond to finance queries, send site communications, and provide general administrative/system support while collaborating with Finance, Site Operations, and Clinical Systems teams.

Coordinate and document protocol-driven clinical trial activities at investigative sites, ensure regulatory and sponsor compliance (ICH-GCP), complete required trainings, conduct subject visits, consent participants, manage laboratory procedures, data entry and query resolution, support recruitment/retention, liaise with study teams and sponsors, and meet enrollment and quality targets.

Lead and oversee clinical research protocols, ensure subject safety and informed consent, maintain regulatory compliance (GCP/FDA), manage investigational product handling, supervise staff training and documentation, and uphold data integrity for study reporting.

Provide front-desk and administrative support for a clinical research site: patient check-in, phone triage, scheduling, meeting coordination, record requests, filing, reports, office supplies and inventory, clinic opening/closing, participant stipend and cash handling, transportation coordination, and general administrative tasks to support clinical staff.

Supports clinical research by assisting with prescreening and patient visits, collecting and recording data in EDC/IVRS, performing phlebotomy and EKGs, managing samples and regulatory binders, completing sponsor and GCP training, and assisting with adverse event reporting and monitoring.

Coordinate and document clinical trial activities per sponsor protocol, FDA and ICH-GCP guidelines. Manage subject visits, consent, data entry/query resolution, safety reporting, lab procedures, training, recruitment/enrollment, and liaison with study teams to meet sponsor targets and maintain regulatory compliance.

Serve as a Sub-Investigator ensuring protocol compliance, subject safety, and data integrity. Perform clinical procedures (physical exams, EKGs, phlebotomy), safety assessments, documentation, and site staff coordination. Maintain licensure, complete required training (GCP/IATA), attend investigator meetings, and support the Principal Investigator in trial-related decisions and subject medical care.

Calculate, reconcile, and report Principal Investigator (PI) fees using sponsor cash receipts, contracts, and patient activity. Prepare PI statements, reconcile with sponsor receipts and clinical activity, extract/analyze data from CRIO and COMTRACK, prepare forecasts and month-end accruals, resolve discrepancies, and collaborate with Finance, Clinical Operations, AR/AP, and PIs.

Lead and oversee clinical research protocols: ensure protocol adherence, subject safety and consent, data integrity, investigational product handling, staff training and oversight, regulatory compliance, and participation in investigator meetings.

Coordinate and execute clinical trial activities at site level per sponsor protocol, FDA and ICH-GCP guidelines. Manage subject visits, consent, data entry, query resolution, AE/SAE reporting, lab procedures, recruitment, sponsor/IRB interactions, and required training to meet enrollment and quality targets.