Jobs at DM Clinical Research

Coordinates clinical research studies at investigative sites, ensuring protocol compliance, accurate documentation, timely data entry, query resolution, patient consent, safety-event reporting, laboratory procedures, participant enrollment, and communication with investigators, sponsors, CROs, and research teams. Requires knowledge of FDA regulations, ICH-GCP guidelines, study protocols, and research documentation. The role includes occasional travel to out-of-town Investigator Meetings.

Manages clinical research studies at investigative sites from first patient visit through closeout. Ensures protocol, FDA, ICH-GCP, SOP, documentation, safety-reporting, consent, data-quality, enrollment, and compliance requirements are met. Trains site teams, prepares for sponsor and CRO visits, maintains essential trial documents, supports patient visits and informed consent, coordinates cross-functional teams, and helps achieve enrollment and operational goals.

Collects and reviews clinical research data to identify inconsistencies, quality issues, and trends affecting study outcomes. Coordinates with regulatory, clinical data, and research site teams; documents action items from site visits, audits, and monitoring; escalates unresolved issues; and maintains query repositories. Ensures compliance with ALCOA+, GDP, GCP, and FDA requirements, reviews clinical source documents, performs root cause analysis, and completes administrative and priority tasks within deadlines.

Provides administrative support for clinical trial site development and integration projects. Responsibilities include maintaining study files, preparing documents and presentations, scheduling meetings, ordering supplies, managing inventory, tracking reports, and supporting correspondence. Requires completion of GCP and IATA training, familiarity with FDA regulations, GCP/ICH guidelines, SOPs, and study protocols. May travel to other sites to perform administrative duties or train new assistants.

Coordinates clinical research studies at assigned sites, ensuring protocol, FDA, ICH-GCP, and sponsor compliance. Conducts participant visits, consent discussions, data entry, query resolution, laboratory procedures, safety-event reporting, and recruitment activities. Maintains study documentation, prepares for sponsor and CRO visits, communicates with investigators and research teams, and supports enrollment goals. Requires ongoing study-specific training and occasional travel to investigator meetings.

Manages clinical study budgets and contracts by reviewing CRO and sponsor proposals, negotiating amendments, tracking financial KPIs, overseeing contract execution, and maintaining accurate systems and reports. Builds relationships with internal stakeholders, vendors, and clinical sites while resolving budgeting challenges, supporting continuous improvement, and handling high-volume assignments in a cross-functional environment.

Coordinates clinical research studies at investigative sites, ensuring protocol, FDA, ICH-GCP, and documentation compliance. Conducts participant visits and consent discussions, manages data entry and query resolution, supports recruitment and retention, oversees adverse-event reporting, coordinates laboratory procedures and supplies, and communicates with investigators, participants, sponsors, CROs, and internal teams. Requires timely training, visit preparation, administrative reporting, and occasional attendance at out-of-town investigator meetings.

Manages clinical trials at investigative sites from study startup through closeout, ensuring protocol compliance, data quality, patient enrollment, safety reporting, documentation, staff training, and adherence to FDA, ICH-GCP, sponsor, and organizational requirements. Conducts informed consent discussions, supports patient understanding, coordinates site and cross-functional teams, prepares for sponsor and CRO visits, maintains essential trial documents, and helps achieve study and site performance goals.

Conduct neurocognitive evaluations, interviews, and clinical ratings of study participants according to research protocols. Assess participants’ functioning and mood, complete testing-related queries, maintain professional communication with sponsors, staff, participants, and families, and manage subjects using strong interpersonal and clinical skills. The role requires continuous learning, accurate documentation, and proficiency with numerous psychiatric and neurocognitive rating scales.

Coordinates clinical research studies at investigative sites, ensuring protocol, FDA, ICH-GCP, and documentation compliance. Conducts participant visits and consent discussions, manages data entry and query resolution, supports recruitment and retention, oversees safety-event reporting, maintains laboratory procedures and study records, and communicates with investigators, participants, sponsors, CROs, and internal teams. Requires at least two years of CRC experience, preferably with industry-sponsored vaccine studies.

Provides administrative and patient-facing support at a clinical research site. Responsibilities include front-desk check-in, phone and email communication, scheduling, meeting coordination, medical record requests, reporting, filing, supplies, shipping, participant stipends, transportation, inventory, cash handling, and clinic opening and closing. Supports site management and clinical staff while maintaining an organized, sanitary, and professional environment.

Conducts clinical trial activities at investigative sites, including subject visits, consent discussions, protocol procedures, data entry, query resolution, recruitment, retention, documentation, laboratory coordination, and communication with research participants, investigators, sponsors, CROs, and internal teams. Ensures compliance with sponsor protocols, FDA regulations, ICH/GCP guidelines, ALCOA-C standards, and study-specific procedures.

Assists clinical research staff with clinical trial activities, including patient visits, data collection, specimen handling and shipment, regulatory documentation, protocol training, source document creation, adverse event reporting, and audit or monitoring issue resolution. Maintains accurate study records and follows FDA regulations, GCP/ICH guidelines, sponsor requirements, organizational SOPs, and study protocols.

Conduct clinical research visits and protocol-required procedures while ensuring compliance with FDA regulations, ICH-GCP guidelines, sponsor protocols, and company SOPs. Manage patient consent, data entry, query resolution, safety event reporting, laboratory procedures, study documentation, recruitment, retention, and enrollment goals. Coordinate with investigators, research participants, sponsors, CROs, laboratories, and internal teams. Attend required meetings and occasional out-of-town investigator meetings.

Conducts clinical trial activities at investigative sites, including subject visits, consent discussions, protocol procedures, data entry, query resolution, safety reporting, laboratory oversight, recruitment, and regulatory compliance. Coordinates with investigators, research participants, sponsors, CROs, laboratories, and administrative teams. Maintains required training, documentation, study knowledge, and site preparedness while supporting enrollment goals. Occasional out-of-town travel for investigator meetings is required.

Coordinate and document clinical trial activities per sponsor protocol, FDA and ICH-GCP guidelines. Manage participant visits, consent, data entry, query resolution, lab procedures, adverse event reporting, enrollment targets, sponsor/IRB interactions, and required training/certifications.

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 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.

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.

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.