Jobs that use informed consent the most include senior clinical scientist, clinical researcher, and senior site manager.
| Rank | Job title | Salary | % of all skills | Job openings |
|---|---|---|---|---|
| 1 | Senior Clinical Scientist | $124,181 | 16% | 96,940 |
| 2 | Clinical Researcher | $55,453 | 12% | 60,864 |
| 3 | Senior Site Manager | $122,901 | 12% | 12,265 |
| 4 | Clinical Research Monitor | $73,325 | 11% | 98,690 |
| 5 | Research Nurse | $53,463 | 11% | 46,665 |
| 6 | Clinical Research Coordinator | $52,459 | 10% | 102,960 |
| 7 | Clinical Trial Coordinator | $50,720 | 10% | 64,859 |
| 8 | Clinical Trials Associate | $74,952 | 9% | 55,487 |
| 9 | Associate Research Specialist | $48,302 | 9% | 56,834 |
| 10 | Clinical Research Administrator | $58,047 | 9% | 143,817 |
What jobs use Informed Consent the most?
1. Senior Clinical Scientist
How senior clinical scientist uses Informed Consent:
- Prepare and manage annual budgets and subcontracts for various NIH fund projects.
- Manage CROs and external investigators.
- Manage pediatric dose development project, technology transfer project and alternate API supplier qualification project on budget and on schedule
Most common skills for senior clinical scientist:
- Informed Consent
- Patients
- Clinical Pharmacology
- Clinical Operations
- Regulatory Agencies
- Patient Care
2. Clinical Researcher
How clinical researcher uses Informed Consent:
- Manage site master file contents and work with sites to ensure communication requirements between site and IRB are adhere to.
- Establish and maintain strong community partnerships to achieve HIV prevention objectives.
- Maintain study database to in compliance with FDA regulations.
Most common skills for clinical researcher:
- Patients
- Informed Consent
- IRB
- Clinical Trials
- Data Collection
- FDA
3. Senior Site Manager
How senior site manager uses Informed Consent:
- Manage non-compliance material returns, QA reports and receiving reports resolving any issues quickly and efficiently.
- Manage computerized time card system including reviewing time cards daily for accuracy to process payroll every week.
- Provide site management support to ensure adherence to FDA regulations, ICH/GCP, and ISO standards.
Most common skills for senior site manager:
- Informed Consent
- Clinical Trial Management
- Clinical Trials
- FDA
- IRB
- QA
4. Clinical Research Monitor
How clinical research monitor uses Informed Consent:
- Manage a consultant to review scientific support and create dossiers on each product that make health claims in the EU.
- Maintain CTMS project tracking system of subject and site information and essential documents.
- Collect and review all initial regulatory documents from site for submission to IRB and sponsor.
Most common skills for clinical research monitor:
- FDA
- Clinical Trials
- Informed Consent
- IRB
- ICH-GCP
- Clinical Operations
5. Research Nurse
How research nurse uses Informed Consent:
- Collect, manage and analyze preliminary data using SPSS statistical software.
- Adhere to local and country specific GCP and ICH guidelines.
- Ensure coordinator and investigator compliance with GCP and ICH guidelines.
Most common skills for research nurse:
- Patients
- Informed Consent
- Data Collection
- IRB
- Oncology
- Research Projects
6. Clinical Research Coordinator
How clinical research coordinator uses Informed Consent:
- Assess study participants for adverse reactions or complications and manage side effects of chemotherapy and other study relate drugs.
- Establish and maintain strong community partnerships to achieve HIV prevention objectives.
- Direct acquisition and analysis of functional MRI research data following GCP and FDA regulations
Most common skills for clinical research coordinator:
- Patients
- Informed Consent
- IRB
- Data Collection
- Research Projects
- Patient Care
7. Clinical Trial Coordinator
How clinical trial coordinator uses Informed Consent:
- Establish and maintain strong community partnerships to achieve HIV prevention objectives.
- Coordinate grant and IRB renewals and submissions; and preparation of publications, study protocols and manuals of operations.
- Develop a GUI tool for volume & surface area of lesion/hematoma/edema in stroke MRI.
Most common skills for clinical trial coordinator:
- Clinical Trials
- Patients
- Informed Consent
- IRB
- Meeting Minutes
- FDA
8. Clinical Trials Associate
How clinical trials associate uses Informed Consent:
- Manage trial master files and study document to meet GCP/ICH and internal guidelines for records retention.
- Audit TMF to ensure all require regulatory documentation are collected and lead.
- Work closely with investigators to recruit eligible patients to clinical protocols, manage data collection and preparation.
Most common skills for clinical trials associate:
- Informed Consent
- Patients
- Clinical Operations
- FDA
- Consent Forms
- TMF
9. Associate Research Specialist
How associate research specialist uses Informed Consent:
- Attain and practice medical insurance information rapidly and correctly; including main carriers and Medicaid.
- Develop an interactive mapping system which utilizes a SAS programming platform and geospatial technology.
- Participate in a summer research intensive that provide hands-on training in interdisciplinary biomedical laboratory techniques with an emphasis in advance instrumentation.
Most common skills for associate research specialist:
- Research Projects
- Informed Consent
- Data Collection
- Laboratory Analysis
- IRB
- Chemistry
10. Clinical Research Administrator
How clinical research administrator uses Informed Consent:
- Manage regional academic and community base oncology practices as the primary contact for all communications and support.
- Ensure effective data management and the following of good clinical practice (GCP) guidelines.
- Initiate the development of standard operating procedures for regulatory compliance monitoring and auditing of regulatory and IRB documentation.
Most common skills for clinical research administrator:
- IRB
- Clinical Research Studies
- Informed Consent
- Principal Investigators
- HIPAA
- FDA
11. Study Coordinator
How study coordinator uses Informed Consent:
- Manage and analyze EKG and sleep data collect from subjects in confidential database.
- Establish and maintain strong community partnerships to achieve HIV prevention objectives.
- Conduct consent discussions and other study procedures per protocol and CFR and GCP guidelines.
Most common skills for study coordinator:
- Patients
- Informed Consent
- IRB
- Data Collection
- FDA
- Clinical Trials
12. Staff Associate
How staff associate uses Informed Consent:
- Manage timely payment of vendors through invoicing (A/R).
- Produce marketing materials to attract new patients, create materials for monthly specials, and manage Facebook account.
- Advocate compliance with all HIPAA, HSE and OSHA policies and procedures.
Most common skills for staff associate:
- Customer Service
- Informed Consent
- Laboratory Tests
- Test Results
- OSHA
- Sops
13. Clinical Research Assistant
How clinical research assistant uses Informed Consent:
- Manage patient caseload with emphasis in occupational rehabilitation
- Maintain compliance with ICH, GCP and federal regulations as well as reporting adverse events to the FDA.
- Perform medical assessment procedures including phlebotomy, laboratory processing, vital signs, and electrocardiogram.
Most common skills for clinical research assistant:
- Patients
- Informed Consent
- Data Collection
- Data Entry
- IRB
- Patient Care
14. Clinical Trials Specialist
How clinical trials specialist uses Informed Consent:
- Manage all clinical data and subject source documentation through the EDC system to verify compliance and subject eligibility.
- Lead study data management activities for oncology trials in preparation for study close-out.
- Review clinical study documents for completeness and compliance with protocol, FDA regulations, ICH and GCP guidelines.
Most common skills for clinical trials specialist:
- Patients
- Clinical Research
- Clinical Trials
- Informed Consent
- FDA
- Consent Forms
15. Clinical Research Specialist
How clinical research specialist uses Informed Consent:
- Manage the input of the subjects' data among various management database including iMedidata, EDC.
- Develop and project manage a staffing program model to support inpatient oncology.
- Manage all planning and execution of oncology clinical trials, domestic and international, including decision impact and companion diagnostic trials.
Most common skills for clinical research specialist:
- Patients
- Clinical Trials
- Informed Consent
- Data Collection
- IRB
- Research Data
16. Research Coordinator
How research coordinator uses Informed Consent:
- Manage participant's records ensuring confidentiality as well as NIH specifications.
- Manage all IRB submissions, sponsor communications, participate in monitoring visits, drug reconciliation and dispensing.
- Recruit, screen, conduct psychometric examinations and collect data for pharmaceutical clinical trials in patients diagnose with Alzheimer's disease.
Most common skills for research coordinator:
- Patients
- Informed Consent
- Data Collection
- IRB
- Research Projects
- Patient Care
17. Senior Clinical Research Scientist
How senior clinical research scientist uses Informed Consent:
- Supervise and manage planning, implementation, conduct and reporting of assign early phase international clinical studies in oncology.
- Contribute to the development of templates for protocols and clinical study reports following FDA, GCP and ICH guidelines.
- Authore and review abstracts, manuscripts, slide decks and posters in collaboration with internal and external (CRO) stakeholders.
Most common skills for senior clinical research scientist:
- Clinical Operations
- Informed Consent
- Clinical Development
- Clinical Trials
- Clinical Data
- Consent Forms
18. Rater
How rater uses Informed Consent:
- Create and manage a file documentation checklist for all UW's and UT's.
- Assess and score the written portion of the TOEFL Jr. exam
- Train and process some DMV tasks to help out the team with the back log.
Most common skills for rater:
- Data Entry
- ESL
- Insurance Policies
- Informed Consent
- Clinical Trials
- Auto Policies
19. Clinical Study Manager
How clinical study manager uses Informed Consent:
- Lead CRA training for Latin American, Asian and European to review GCP and protocol training.
- Manage projects relate to commercialization and post market analysis for abdominal aortic aneurysm repair grafts as guided by FDA regulations.
- Participate in CRF (EDC) design and CCG preparation.
Most common skills for clinical study manager:
- GCP
- Informed Consent
- Oversight
- Clinical Operations
- ICH
- Data Management
20. Clinical Research Associate
How clinical research associate uses Informed Consent:
- Manage, schedule and train up to 15 CRAs.
- Recruit patients, attain patient inform consent form, educate subjects on compliance, and ensure patient safety per ICH guidelines.
- Manage site TMF to ensure communication requirements adherence
Most common skills for clinical research associate:
- Patients
- Informed Consent
- CRA
- Clinical Trials
- Clinical Trial Management
- Oncology
Other skills
- I-9 career
- IAM career
- ICU career
- IDS career
- IEP career
- IEPs career
- III career
- ILS career
- IP career
- IPC career
- IRB career
- IRS career
- ISR career
- ITIL career
- IV career
- In-Home career
- In-Room career
- Inbound Calls career
- Incident Management career
- Incident Reports career
- Incident Response career
- Income Tax Returns career
- Independent Living career
- Individual Tax Returns career
- Individual Therapy career
- Individual Training career
- Industrial Cleaning career
- Industrial Design career
- Industrial Maintenance career
- Infection Control career
- Infection Prevention career
- Infectious Disease career
- Informed Consent career
- Infrastructure career
- Inspection Reports career
- Inspection Results career
- Instagram career
- Instructional Design career
- Instructional Materials career
- Instructional Program career
- Instructional Strategies career
- Instructional Support career
- Insurance Benefits career
- Insurance Carriers career
- Insurance Claims career
- Insurance Coverage career
- Insurance Eligibility career
- Insurance Fraud career
- Insurance Policies career
- Insurance Products career
- Insurance Sales career
- Insurance Verification career
Updated December 28, 2023