Jobs at DM Clinical Research

Manages clinical research sites from study start through closeout, ensuring protocol adherence, FDA and ICH-GCP compliance, data quality, enrollment, patient retention, staff performance, training, documentation, and sponsor readiness. Conducts informed consent discussions, coordinates communication among patients and research teams, implements site procedures, tracks goals, and submits required administrative documentation. Requires clinical research coordination and management experience, strong clinical systems knowledge, and excellent communication skills.

Manages clinical research sites from study start through closeout, ensuring protocol compliance, data quality, patient retention, enrollment, staff performance, training, and regulatory adherence. Oversees site operations, sponsor and CRO visits, documentation, reporting, and implementation of study procedures. Supervises and develops site staff, communicates organizational goals, conducts patient consent discussions, and supports effective coordination among patients, healthcare providers, sponsors, and research teams. Occasional travel to investigator meetings is required.

Lead regional clinical operations across multiple research sites to ensure trial execution, enrollment, regulatory compliance, quality, financial performance, and operational consistency. Coach site leadership, drive site activation and growth, analyze KPIs, mitigate operational risks, and align regional activities with organizational strategy.

Support vendor onboarding, site readiness, and operational projects across a national clinical research site network. Coordinate vendor communications, maintain trackers and documentation, assist with PBMC qualification and laboratory readiness, support site builds/expansions, perform follow-up and escalation, prepare project materials, and travel to sites as needed to ensure consistent workflows and compliance.

Assist clinical research staff with executing clinical trials: complete required trainings, collect and record patient data in EDC, collect/manage/ship specimens, conduct patient visits, maintain regulatory binders and source documents, assist adverse event reporting and monitoring/audit responses, and support other study tasks as assigned.

Support accounts receivable functions including invoice generation and review, payment reconciliation, collections, reporting, contract analysis, resolving discrepancies, and customer communications.

Coordinate psychiatry clinical trials by conducting study visits, consent, data entry, query resolution, safety reporting, protocol adherence, training completion, and liaison with sponsors, labs, and investigators to meet enrollment and quality metrics.

Coordinate and document clinical trial activities at site level per protocol, FDA and ICH-GCP standards. Complete required trainings, conduct subject visits and consent, manage data entry and query resolution, liaise with sponsors/CROs, support lab procedures, and assist recruitment and retention.

Coordinate and oversee clinical trial conduct at assigned investigative sites ensuring compliance with sponsor protocols, FDA and ICH-GCP guidelines. Manage subject visits, data entry and query resolution, lab procedures and inventory, safety reporting (AEs/SAEs), recruitment/enrollment goals, site documentation, and sponsor/CRO communications. Train and mentor site staff and prepare sites for monitoring and investigator meetings.

Manage clinical trials at assigned investigative sites ensuring compliance with sponsor protocol, FDA and ICH-GCP guidelines. Oversee site readiness, training, enrollment, data quality, AE reporting, consenting, and study documentation from first patient first visit through closeout while coordinating cross-functional teams.

Manage dispensing and accountability of investigational products for clinical trials: compound/prepare IP per protocol, ensure blinding and storage, maintain regulatory and IP records, audit clinical data, train and onboard staff, develop SOPs/workflows, and coordinate with investigators and sponsors.

Coordinate and conduct protocol-driven clinical study visits, ensure regulatory and ICH-GCP compliance, complete required trainings, perform timely data entry and query resolution, manage lab procedures and safety reporting, support enrollment and retention, liaise with sponsors/CROs and site teams, and oversee informed consent and participant communication.

Coordinate site clinical research activities per sponsor protocol, FDA and ICH/GCP guidelines: conduct subject visits, data entry and query resolution, consent discussions, lab handling, training completion, recruitment/retention, and liaison among site, sponsor, and study teams.

Manage clinical studies at investigative sites ensuring protocol, FDA and ICH-GCP compliance. Oversee site training, visit preparedness, data quality, adverse event reporting, enrollment targets, and study close-out. Coordinate with cross-functional teams and site leadership and complete required certifications and electronic systems training.

Dispense and manage investigational products per sponsor protocols, maintain IP accountability and storage, perform data audits, train and support team members, ensure regulatory compliance and site documentation, and collaborate with investigators and sponsors on protocol execution.

Serve as a Sub-Investigator (Nurse Practitioner) to ensure protocol adherence, protect subject welfare, perform clinical assessments and procedures, manage site clinical staff activities, document study events, and participate in investigator meetings per FDA/GCP regulations.

Coordinate and document clinical trial activities at assigned sites per sponsor protocol, FDA and ICH-GCP guidelines; manage subject visits, consent, data entry, query resolution, safety reporting, training, lab procedures, enrollment targets, and liaison with sponsors, CROs, and site teams.

Provide clinical oversight and conduct study-related medical procedures for research subjects, ensure protocol and regulatory compliance, manage subject care and documentation, assist the Principal Investigator, supervise clinical staff, complete required trainings, and attend investigator meetings.

Dispense, compound, and manage investigational products per sponsor protocols; maintain IP accountability and storage; audit clinical data; support site startup, training, regulatory documentation, and coordinate with investigators and sponsors to ensure protocol compliance.

Lead day-to-day HR service delivery and employee relations across a geographically dispersed workforce. Oversee HR operations, HRIS/data integrity, compliance, policies, leaves, investigations, onboarding/separations, and HR projects. Coach leaders, manage case documentation, improve HR workflows and controls, partner with cross-functional teams, and supervise HR staff to ensure consistent, timely, and compliant people practices.