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Clinical Research Coordinator II CYNET SYSTEMS
Somerset, NJ2 days ago
- $23–$28 Per Hour
- Temporary
- Contractor
- Part-time
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Skills
- Auditingunmatched
- Budget Managementunmatched
- Cardiac Monitoringunmatched
- Case Report Form (CRF)unmatched
- Clinical Assessmentunmatched
- Clinical Dataunmatched
- Clinical Practices/Protocolsunmatched
- Clinical Researchunmatched
- Clinical Trialunmatched
- Data Qualityunmatched
- Detail Orientedunmatched
- Documentationunmatched
- Electrocardiogramunmatched
- Electronic Data Capture (EDC)unmatched
- GCP (Good Clinical Practices)unmatched
- High School Diplomaunmatched
- Identify Issuesunmatched
- Informed Consentunmatched
- Interpersonal Skillsunmatched
- Laboratory Analysisunmatched
- Laboratory Testingunmatched
- Logisticsunmatched
- Maintain Complianceunmatched
- Medical Recordsunmatched
- Medical Terminologyunmatched
- Medicineunmatched
- Microsoft Access Databaseunmatched
- Microsoft Excelunmatched
- Microsoft Officeunmatched
- Microsoft Outlookunmatched
- Microsoft Windows Operating Systemunmatched
- Microsoft Wordunmatched
- Operations Processesunmatched
- Organizational Skillsunmatched
- Paint Shop Pro Tubesunmatched
- Project Scheduleunmatched
- Quality Controlunmatched
- Quality Managementunmatched
- Quality Metricsunmatched
- Record Keepingunmatched
- Regulationsunmatched
- Research Protocolsunmatched
- Sample/Specimen Processingunmatched
- Specimen Collectionunmatched
- Staff Trainingunmatched
- Standard Operating Procedures (SOP)unmatched
- Telemetryunmatched
- Time Managementunmatched
- Training/Teachingunmatched
Description
Job Title: Clinical Research Coordinator
Job Type: Contract
Duration: 3 Months
Location: Somerset, NJ 08873
100% Onsite role
Part-time role 20 Hours/Week (Hours are flexible, but based on site need.)
SUMMARY:
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning.
RESPONSIBILITIES:
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:
ADDITIONAL SKILLS/QUALIFICATIONS:
Job Type: Contract
Duration: 3 Months
Location: Somerset, NJ 08873
100% Onsite role
Part-time role 20 Hours/Week (Hours are flexible, but based on site need.)
SUMMARY:
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning.
RESPONSIBILITIES:
- Provide clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols
- Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data
- Attend all relevant study meetings
- Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research
- Recruit and screen patients for clinical trials and maintain subject screening logs
- Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits
- Design and maintain source documentation based on protocol requirements; Schedule and execute study visits and perform study procedures
- Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness
- Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics
- Monitor subject safety and report adverse reactions to appropriate medical personnel
- Correspond with research subjects and troubleshoot study-related questions or issues
- Participate in ?huddles? to confirm daily study tasks are assigned to team members and are executed to the expected standards
- Assist with study data quality checking and query resolution.
- Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.
- Record, report and interpret study findings appropriately to develop a study-specific database.
- Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.
- Provide training to new investigator site staff members on study-specific topics and requirements.
- Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
- Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
- Assist research site with coverage planning related to staffing and scheduling for research projects.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:
- Knowledge of clinical trials In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules Knowledge of medical terminology
- Skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
- Excellent interpersonal skills
- Ability to pay close attention to detail Ability to establish and maintain effective working relationships with coworkers, managers and clients
ADDITIONAL SKILLS/QUALIFICATIONS:
- Coordinator tasks, patient visits, recruitment, query resolution, EDC.
- High school diploma (A BS would be a plus) or educational equivalent and relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience
- Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies
Numbers & Facts
| Location | Somerset, NJ |
| Industry | Other/Not Classified |
| Salary | $30.48 Per Hour |
| Company Size | 100 to 499 employees |
| Year Founded | 1998 |
| Website | www.eteaminc.com |
About Company
Looking for a great job? Join eTeam. We’re looking for talented staffing professionals to join our staff. We also provide contract assignments and full-time jobs at Fortune 2000 Companies. We’ve been named one of the best companies to work for by Staffing Industry Analysts and New Jersey Business.
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