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# Google IT Automation with Python

- **Company:** CareerCircle
- **Location:** Newark, NJ, United States
- **Salary:** $66,560.0 - $76,960.0
- **Contract:** Temporary contract
- **Skills:** Microsoft Word, Microsoft Excel, Artificial Intelligence, Data Analysis, Software Applications, Databases, Computer Literacy, Data Security, Data Warehousing, Document Management Systems, Microsoft Office, Microsoft PowerPoint, Web Application Security, Custom Reports
- **Published:** July 9, 2026
- **Apply:** https://www.careercircle.com/jobs/all/all/usa/nj/newark/ed7b58e8-9121-4140-9312-4b6f3808e284

## About the Role

* Minimum 3 years of relevant clinical research experience, preferably in a clinical research coordinator or similar role.
 * Hands-on experience with clinical research coordination, including patient screening, recruitment, and enrollment.
 * Experience working in oncology clinical research or strong interest in oncology trials.
 * Proficiency with computer software programs such as Excel and Word, with the ability to create and manage study tools and reports.
 * Bachelor's degree required.
 * Familiarity with Good Clinical Practice guidelines and regulatory requirements governing clinical trials., Data Analysis
Data Security
Detail Oriented
Microsoft Excel
Risk Management
Compliance Risk
Microsoft Office
Ad Hoc Reporting
Data Warehousing
Analytical Skills
Quality Assurance
Loan Documentation
Workflow Management
Microsoft PowerPoint
Credit Risk Management
Business Administration
Web Application Security
Document Management Systems
Standard Operating Procedure
Ethical Standards And Conduct
Customer Relationship Management
+0, Auditing
Coaching
Teamwork
Aviation
Budgeting
Mechanics
Scheduling
Operations
Management
Cleanliness
Communication
Team Oriented
Accountability
Diesel Engines
Cooling Systems
Health Advocacy
Customer Service
Safety Standards
Computer Literacy
Workflow Management
Operation Maintenance
Artificial Intelligence
Discounts And Allowances
Authorization (Computing)
Employee Assistance Programs
Key Performance Indicators (KPIs)
Commercial Driver's License (CDL)
Automotive Service Excellence (ASE) Certification
Security Identification Display Area (SIDA) Badge
+0

## Description

Oncology
Auditing
Research
Visionary
Innovation
Checklists
Registration
Microsoft Excel
Clinical Trials
Medical Records
Data Collection
Informed Consent
Clinical Research
Case Report Forms
Multicenter Trial
Human Subject Research
Artificial Intelligence
Clinical Trial Protocols
Engineering Design Process
Medical History Documentation
Good Clinical Practices (GCP)
Clinical Research Coordination
Institutional Review Board (IRB), * Coordinate the initiation and activation of new clinical trial protocols, ensuring all required approvals are in place before study activation, including Scientific Review Board, Institutional Review Board, Human Research Oversight Committee, data collection plans, and finance/contract approvals.

 * Prepare and organize study tools such as study binders, medication diaries, eligibility checklists, calendars, and flow sheets as required for each protocol.
 * Use Oncore, Excel, and Word to develop and maintain study tools, including eligibility checklists, medication diaries, calendars, and flow sheets tailored to specific trials.
 * In collaboration with the Research Nurse Clinician and/or physician, review patients' charts and medical histories to confirm protocol eligibility and obtain necessary source documents from the medical record.
 * Under the direction of the Research Nurse Clinician and/or physician, ensure that the IRB-approved informed consent form is properly obtained, signed, filed in the medical record, and that a copy is provided to the patient.
 * Register consented research patients with the appropriate study sponsors, including industry partners and cooperative groups, and enter all required information into the Oncore clinical trials database.
 * Maintain complete and accurate research records for all enrolled patients, including consent forms, eligibility documentation, case report forms, registration confirmations, and corresponding source documents across multiple clinical locations.
 * Support and coordinate patient screening, recruitment, and enrollment activities for assigned clinical trials, ensuring adherence to protocol-specific inclusion and exclusion criteria.
 * Assist, in collaboration with the Research Nurse Clinician and physician, with grading adverse events using the most recent National Cancer Institute common toxicity criteria or protocol-specific grading scales.
 * Complete Serious/Unexpected Adverse Event forms for internal and multicenter serious or unexpected adverse events in accordance with study sponsor requirements, federal regulations, and institutional guidelines.
 * Ensure that all research records remain up to date and audit-ready for all patients enrolled on clinical trials, including those at main centers, community physician offices, and affiliated hospitals.
 * Generate and provide regular reports from Oncore to tumor study group members and Principal Investigators on the status of assigned studies and enrolled subjects.
 * Serve as a primary liaison with study sponsors, schedule monitoring visits and conference calls, and provide accurate and timely responses to sponsor queries.
 * Understand and anticipate the needs of study sponsors to facilitate efficient study conduct and strong collaborative relationships.
 * In collaboration with the Research Nurse Clinician, help ensure that all personnel involved in the study, including investigators, conduct the trial in accordance with the protocol, Good Clinical Practice guidelines, and institutional policies.
 * Communicate clearly and professionally with patients, clinical teams, and study stakeholders to support patient understanding, adherence, and a positive trial experience., Union Beach, NJ*On-Site
Research
Chemistry
Visionary
Innovation
Collections
Scale (Map)
Food Science
Distillation
Wet Chemistry
Detail Oriented
Beverage Products
Technical Management
Laboratory Equipment
Artificial Intelligence
Engineering Design Process
Good Laboratory Practice (GLP)
Gas Chromatography Mass Spectrometry


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