May perform initial data entry of ICSRs (review, extract, accurately enter AE data from ICSR reports). * May interpret case-related information including medical conditions, lab results and ...
May perform initial data entry of ICSRs (review, extract, accurately enter AE data from ICSR reports). * May interpret case-related information including medical conditions, lab results and ...
Entry Level Icsr information
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$12.26 - $18.95
7% of jobs
$18.95 - $25.63
4% of jobs
$25.63 - $32.32
3% of jobs
$38.25 is the 25th percentile. Wages below this are outliers.
$32.32 - $39.01
12% of jobs
The median wage is $44.20 / hr.
$39.01 - $45.69
31% of jobs
$45.69 - $52.38
15% of jobs
$54.36 is the 75th percentile. Wages above this are outliers.
$52.38 - $59.07
12% of jobs
$59.07 - $65.76
0% of jobs
$65.76 - $72.44
9% of jobs
$72.44 - $79.13
5% of jobs
$79.13 - $85.82
2% of jobs
$12
$49
$85
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What is the difference between Entry Level Icsr vs Entry Level Clinical Data Coordinator?
| Aspect | Entry Level Icsr | Entry Level Clinical Data Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, basic understanding of clinical trials, regulatory knowledge | Bachelor's degree, familiarity with clinical data management systems |
| Work Environment | Pharmaceutical companies, CROs, clinical trial sites | Research organizations, pharmaceutical companies, CROs |
| Industry Usage | Regulatory submissions, adverse event reporting | Data entry, database management, quality control |
Entry Level Icsr roles focus on safety reporting and regulatory compliance, while Entry Level Clinical Data Coordinators handle data management and database tasks. Both positions require a similar educational background and work in clinical research settings, but they differ in daily responsibilities and specific skill sets.
What jobs pay $2000 a day?

Job description
- Sets work priorities and direction with input from Manager.
- Responsible for the accurate and timely book-in and acknowledgement of adverse event information in compliance with applicable SOPs and guidelines.
- Understand SDEA and global regulatory reporting timelines in order to prioritize cases if needed.
- Perform simple queries of the safety database, e.g. duplicate searches.
- Maintain and manage dept. Safety mailbox, distributing to relevant parties as applicable.
- May perform initial data entry of ICSRs (review, extract, accurately enter AE data from ICSR reports).
- May interpret case-related information including medical conditions, lab results and procedures, as well as compile complete narrative summaries.
- Meet specific data and quality targets for case handling
- Assist with tracking and reconciliation of incoming adverse event reports.
- Coordinate submission of product complaints to the Quality assurance department.
- Participate in department projects, as required and will be cross-trained to handle other functions as deemed necessary
- Recognizes situations that require assistance from more senior staff members and seeks assistance from appropriate internal and external resources.
- Assists Safety Specialists in sending and tracking follow-up letters.
- Remain current with case handling SOPs, guidance documents and database technology
- May assist manager in the preparation of training material and assist in training new employees their functional area.
- May assist manager with writing/reviewing guidelines for their functional area of expertise.
- May assist with other projects as necessary (i.e., study unbinding, reconciliation with vendors, etc)
- Ensures departmental workflow processes and timelines are followed
- Knowledge, Experience and Skills:
- Excellent interpersonal communication skills, both written and oral
- Excellent computer skills in Microsoft environment (Microsoft Excel, Power point and Word).
- Safety database and data entry experience preferred
- Basic understanding of medical and drug terminology preferred
- JD - Drug Safety & Public Health, Operations
- Knowledge and experience with safety reporting and regulatory compliance and experience with international safety reporting/regulations is preferred
- Demonstrates initiative, teamwork and accountability
- Demonstrated success working both independently and in collaboration with others
- A quality driven individual with strong attention to detail and accuracy is required
- Strong organizational skills, and ability to adapt to change
- A demonstrated ability to manage own workload, prioritize, plan and organize assignments and work under stick timelines is required.
- Ability to follow guidelines and procedural documents
- AA or BS degree (or equivalent experience) and little to no experience.
- Industry experience in the health, clinical, bio-pharmaceutical, or relevant industries such as, pharmacy technician, nursing assistant is valuable but not required.
All your information will be kept confidential according to EEO guidelines.
About Integrated Resources
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Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996