...research in the physical sciences.
We are seeking to fill a Document Management Specialist position!
This position serves a key role in facilitating... ...system.
Support and facilitate development and review, and conduct monitoring of, the Laboratory’s suite of Institutional...
Suggested
Full time
Contract work
For contractors
Remote job
Work visa
Flexible hours
Shift work
Afternoon shift
...engineers and gauge owners
Responsible for conducting multiple reviews for conformance
Perform database queries regarding usage of... ...role is desired
Proven experience with complex documentation management and database driven computer systems is desired...
Suggested
Shift work
...Coding and Documentation Specialist - Population Health
Be a part of our talented and growing team!
Are you looking for a Full-Time Coding... ...part of our clinical operations, your duties will include:
Review and analyze medical records to ensure accurate coding based...
Suggested
Full time
Private practice
Local area
Relocation bonus
Monday to Friday
...to Company growth, we are actively seeking an experienced Document Control Specialist to join our team in New Jersey.
Responsibilities &... ...control and flow of engineering design/submittals and processes/reviews
Implement master tracking of all packages/deliverables...
Suggested
...The Opportunity
Description
We're looking for a Document Control , working in Biotechnology/Medical Devices industry... ...may include filing, copying, and scanning.
Work may include review of documents and the document control flow in the Master Control...
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The Data Reviewer, Office of Data Reliability (ODR) is accountable for critical review of pre-submission applications ready for regulatory... ...Responsibility
Ensures compliance with cGMP/cGLP and good documentation procedure during the review process
Audits regulatory pre-...
Suggested
Immediate start
...in healthcare providing research and innovation to drive the future of medical treatments. They are seeking an experience Medical Reviewer to ensue scientific accuracy and clinical appropriateness and validity of promotions materials.
Salary/Hourly Rate:
$50 - $60/hr
Position...
Suggested
Hourly pay
...role reporting directly to the Clinical Document Team Manager (CDTM). The Clinical Document... ...work completed by the Clinical Document Specialist (CDS) Team. As a senior employee, the... ...Responsibilities:
* Responsible for review of study documentation for Trial Master...
Suggested
Local area
...recruiter.
The Opportunity
Description
We're looking for an eTMF Reviewer I , working in Pharmaceuticals and Medical Products industry... ..., New Jersey, United States .
Job description:
Reviewing documents for quality review that are in company's eTMF system in the Functional...
Suggested
$60 - $63 per hour
...Proclinical is seeking a Medical Reviewer who will play a crucial role in ensuring the scientific... ....
The Medical Promotional Review Specialists responsibilities will be:
Review... ....
Review, provide comments, and document verdicts for all assigned promotional materials...
Suggested
Hourly pay
Contract work
...The Middlesex County Office of Planning is seeking a qualified candidate to serve as Assistant Planner in its fast-paced Development Review division. The Assistant Planner will be responsible for preparing staff reports on subdivision and site plan applications,...
Suggested
...of multiple myeloma.
Legend Biotech is seeking a QC Data Reviewer as part of the Quality team based in Raritan, NJ.
Role... ...•Utilization of electronic systems (LIMS) for execution and documentation.
•Create, review, and approve relevant QC documents, SOP's...
Suggested
Work experience placement
Immediate start
Shift work
Night shift
Afternoon shift
...with the CEO of Gan & Lee Pharmaceuticals USA. The Sr. Manager, Document Management supports all Controlled Document Management at the... ...Policies, Forms and Work Instructions
Knowledge/Regulation:
Review SOPs, Policies, and Work Instructions for compliance with GCP...
Suggested
..., dedicated individual committed to work under the highest ethics standards for the following position:
Project Manager for CQV Documentation Project
Qualifications: Bachelor's Degree in Science or Engineering.
Minimum of 5 years of experience in Project Management in direct...
Suggested
Holiday work
Immediate start
Weekend work
...We are hiring a Document Control Clerk / Filing Specialist for one of our clients in New Brunswick, NJ .
Job Description:
~ Filing, copying, collating, phones
Skills required:
Pleasant, able to deal with difficult consumers
Typing,...
Suggested
Casual work
Remote job
...with-us.
Position Summary
To coordinate and author complex documents needed for regulatory submissions, ensuring the coordination... ...internal and external processes and guidelines while managing the review process and, on an ongoing basis, resolve issues, errors, or...
Remote job
Worldwide
Shift work
Assistant Document Control needs 1 to 3 years of relevant experience in the pharmaceutical/biopharmaceutical industry
Assistant Document Control requires:
BA/BS degree or equivalent experience is preferred.
1 to 3 years of relevant experience in the pharmaceutical...
...Registry Cards. Working with other departmental personnel, the document coordinator will maintain and file records, as well as... ...Quality Assurance, and Quality Control, to complete the process of reviewing, logging, and filing documents.
· Ensure accurate entry of the...
Remote job
Contract work
Local area
...we work every day is important to us.
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Performs critical in-depth review of all scientific data for Quality Control laboratory documents under general supervision.
Under the direction of QA management, this individual:
* Performs...
Contract work
Temporary work
Local area
Immediate start
Flexible hours
Senior Business Analyst (Documentation/data)
Berkeley Heights, NJ
Do you thrive on translating complex data into clear, concise documentation... ...results in test environments.
Technical Documentation Specialist: Focus on creating comprehensive technical documentation, including...