Director, Project Physician - (Job Number: 0806159) |
| Director, Project Physician - (Job Number: 0806159) DescriptionJohnson and Johnson P... |
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Senior Scientist - (Job Number: 0805966) |
| Senior Scientist - (Job Number: 0805966) DescriptionThe Johnson & Johnson Consumer and P... |
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Senior Regulatory Affairs Specialist - (Job Number: 0806030) |
| Senior Regulatory Affairs Specialist - (Job Number: 0806030) DescriptionEthicon, Inc, a ... |
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Regulatory Affairs Associate Director - (Job Number: 0806020) |
| Regulatory Affairs Associate Director - (Job Number: 0806020) DescriptionJohnson & J... |
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Regulatory Affairs Associate - (Job Number: 0805693) |
| Regulatory Affairs Associate - (Job Number: 0805693) DescriptionJohnson & Johnson C... |
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Associate Director, Primary Market Research - (Job Number: 0806105) |
| Associate Director, Primary Market Research - (Job Number: 0806105) DescriptionEthicon, ... |
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Field Marketing Manager (1 of 5 positions) - (Job Number: 0806073) |
| Field Marketing Manager (1 of 5 positions) - (Job Number: 0806073) DescriptionDePuy S... |
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| Process Improvement Leader - (Job Number: 0806013) Description Johnson & Johnson C... |
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Information Technology Lead, Sales Solutions Technology - (Job Number: 0805900) |
| Information Technology Lead, Sales Solutions Technology - (Job Number: 0805900) D... |
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| SAP MDM PROGRAM MANAGER - (Job Number: 0805706) DescriptionJohnson & Johnson Consumer P... |
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Clinical Research Associate - CRA I - monitoring exp required - temp-to-hire!
| Details |
Country: USA
Location: New Jersey-Central North Brunswick, NJ
Total applied: 46 |
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Clinical Research Associate - CRA I - monitoring exp required - temp-to-hire!
Kelly Clinical Research is seeking a CRA I (Clinical Research Associate, level 1) for a contract role at a pharmaceutical and medical device company. This position may be contract-to-hire for the right individual. The position will be based in North Brunswick, NJ.Job Duties: The incumbent will be responsible for one or more concurrent clinical study from start-up to closeout. This role will specifically include tasks focused on: Site qualification and initiation Routine site visits, as necessary, as monitor and compliance representative Clinical and regulatory documentation (drafting, tracking, maintaining and auditing clinical documentation), incl. work with protocol, CRFs, SOPs, etc. Clinical operations tasks in budgeting, timelines, supplies, adverse events, etc.On-call support and ongoing training for investigator sitesRegulatory support for submissions and reportingThis position will have up to 25% travel.Job Requirements:BA/BS required, with degrees in health or sciences preferred1 year of clinical research experience required6 months of clinical monitoring experience requiredHighly conversant in FDA regulatory requirementsStrong written communication skillsQUALIFIED APPLICANTS ARE ENCOURAGED TO CLICK "APPLY NOW" FOR IMMEDIATE CONSIDERATION!Kelly Scientific Resources®(KSR) is the scientific business unit of Kelly Services, a Fortune 500 staffing industry leader. We provide scientific staffing services on a temporary, project and full-time basis to a broad spectrum of industries including Pharmaceutical, Biomedical, and Clinical Research. Learn more about company
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