Jobs at Evolution Research Group

Supports Phase I-IV clinical trials by dispensing investigational medications, performing vital signs, venipuncture, ECGs, point-of-care testing, specimen processing, documentation, and sample shipment. Maintains compliance with research protocols, GCP, ICH guidelines, site procedures, safety requirements, and regulatory standards while working collaboratively in a clinical research unit.

Manages daily administrative, financial, recruiting, regulatory, and operational activities for clinical research sites. Coordinates study feasibility, budgets, contracts, affiliate physicians, patient recruitment, regulatory compliance, database support, staffing, payroll, and sponsor obligations. Supervises multiple departments and collaborates with clinical research coordinators to ensure efficient study initiation, enrollment, documentation, and execution in accordance with GCP, ICH, FDA, and company requirements.

Supports Phase I-IV clinical trials by preparing source documents, conducting vitals, ECGs, and phlebotomy, entering patient visit data, managing lab kits, processing and shipping specimens, completing protocol training, and performing general administrative tasks. Ensures compliance with study protocols, FDA regulations, GCP, ICH guidelines, and company procedures. Requires strong organization, communication, attention to detail, medical terminology knowledge, and willingness to work night shifts.

Manages clinical research projects from study start-up through completion, overseeing scope, budgets, timelines, protocols, study documents, vendors, regulatory compliance, and client communications. Leads multidisciplinary teams, coordinates sites and sponsors, reviews clinical data and monitoring reports, supports FDA inspections, and ensures deliverables meet protocols, SOPs, contracts, and quality expectations. Provides therapeutic training and contributes to organizational initiatives.

Manages clinical research projects from study start-up through closeout, overseeing scope, budgets, timelines, vendors, documentation, regulatory compliance, data review, and client communications. Leads multidisciplinary teams, supports protocols and clinical study reports, coordinates investigational materials and site activities, ensures adherence to contracts, SOPs, and regulations, and participates in inspections, training, meetings, and conferences.

Leads clinical research project teams and oversees budgets, timelines, deliverables, risks, quality, change control, client relationships, and regulatory compliance. Serves as an escalation point for sponsors and cross-functional teams, reviews project KPIs, approves project plans and reports, supports staffing and process governance, and may directly manage clinical projects. Provides guidance and training to project managers while ensuring milestones are achieved.

Coordinates Phase I-IV clinical trials by reviewing protocols, preparing study documents, screening and enrolling participants, obtaining informed consent, scheduling visits, maintaining accurate records, entering data, tracking adverse events, and supporting study closeout. Ensures compliance with FDA regulations, Good Clinical Practice, ICH guidelines, institutional review board requirements, and company procedures while supporting participant safety and data integrity.

Coordinates and manages Phase I-IV clinical trials under Principal Investigator and Site Director supervision. Responsibilities include protocol implementation, participant screening and enrollment, informed consent, study visits, regulatory and IRB documentation, source records, CRF completion, medication dispensing, adverse event tracking, sponsor communication, monitoring visits, and study closeout. The coordinator ensures protocol compliance, data integrity, participant safety, and adherence to FDA, GCP, ICH, and company requirements while mentoring support staff.

Performs accurate clinical data entry and processing for research studies, maintains confidential participant records, tracks completion of study data and visits, quality-controls clinical information, reports discrepancies, and assists with resolving data queries. Follows study protocols, company procedures, Good Clinical Practice, and ICH guidelines while coordinating with site staff, sponsors, CROs, and data managers.

Assists Clinical Research Coordinators with Phase I-IV clinical trial execution, including data collection, informed consent, adverse event reporting, participant communication, venipuncture, vital signs, ECGs, procedure setup, protocol compliance, and emergency support. Coordinates with clinical departments, maintains study supplies and documentation, reviews schedules and flowsheets, attends study meetings, and follows applicable GCP, ICH, HIPAA, OSHA, and organizational requirements.

Enters, updates, verifies, and maintains high volumes of sensitive healthcare data. Prepares reports and correspondence, protects confidential information, handles frequent phone communication, resolves data discrepancies, and collaborates with clinical and administrative teams to support accurate records and efficient workflows.

Manages clinical research projects from start-up through completion, overseeing scope, budgets, timelines, study materials, vendors, sites, regulatory compliance, data review, reporting, and client communications. Leads multidisciplinary internal and external teams, develops protocols and clinical documents, reviews monitoring reports, supports inspections, and ensures deliverables meet contractual, protocol, SOP, and quality requirements. The role is fully remote with occasional off-site meetings and conferences.

The TMF Specialist manages, reviews, approves, and files clinical trial documents in the eTMF. Responsibilities include validating metadata and version control, maintaining Expected Documents Lists, monitoring completeness, supporting audit readiness, resolving document discrepancies, coordinating with stakeholders, and ensuring compliance with SOPs, GCP, ICH guidelines, and TMF standards.

Supports clinical operations by organizing and quality-checking trial master files, preparing regulatory and study documents, coordinating meetings and training, tracking site activity, enrollment, monitoring reports, and study progress, and entering clinical data. The role assists with study drug release, investigator meetings, site communications, shipments, and issue escalation while ensuring compliance with SOPs, FDA regulations, and ICH/GCP guidelines.

Assists with Phase I-IV clinical trials by dispensing investigational and routine medications, performing vital signs, venipuncture, ECGs, point-of-care testing, and biological specimen processing. Maintains accurate subject documentation, specimen accountability, storage, shipping, and disposal while following written orders, site procedures, safety precautions, GCP, ICH guidelines, and regulatory requirements.

Assists with Phase I–IV clinical trial execution by dispensing investigational medications, collecting biological samples, performing venipuncture, vital signs, ECGs, point-of-care tests, specimen processing, documentation, and maintaining protocol and Good Clinical Practice compliance.

The Staff Accountant manages accounts payable and receivable, site cash boxes, payroll, and employee time-off requests. The role also supports employee onboarding and offboarding, building access management, and administrative coordination. Success requires strong organization, confidentiality, attention to detail, communication, time management, basic computer skills, and familiarity with clinical research regulations, GCP, ICH guidelines, and medical terminology.

Administers and scores psychometric tests for clinical trial participants, ensuring accurate data collection, protocol compliance, ethical conduct, and confidential documentation. Reviews study protocols, coordinates rating activities with investigators, sponsors, and training representatives, assists with participant recruitment and prescreening, collects medical and psychiatric histories, and documents informed consent. Maintains required licensure and follows FDA regulations, Good Clinical Practice, and company procedures.

Assist with launching and operating a CLIA-certified, GLP-compliant clinical research safety laboratory supporting Phase I studies. Responsibilities include supervising personnel, coordinating testing workflows, maintaining quality and compliance systems, supporting inspections and audits, managing assays, samples, supplies, equipment, and data reporting, and collaborating with sponsors and clinical teams.

The Sub-Investigator serves as the secondary physician or nurse practitioner overseeing clinical and medical activities at a research site. Responsibilities include evaluating and executing clinical trials, ensuring protocol and GCP/ICH compliance, managing subject care and adverse events, maintaining informed consent and regulatory documentation, supporting recruitment, liaising with sponsors and IRBs, overseeing investigational products, participating in audits, and ensuring accurate clinical data and reporting.