Investigator Support Associate
Covance (Singapore)
appropriate information and informing personnel of additional testing needs. 2. Acts as a liaison for investigator sites and sponsors; communicates investigator site needs when new policies or procedures are discussed. 3. Effective and timely ...Notes are only visible to you.
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Senior Specialist, Site Contracts, GSS
Covance (Singapore)
Business Title Senior Specialist, Site Contracts, GSS Requisition Job Category Clinical Research Locations Singapore ... up and maintenance phases of all allocated studies. Provide direct support to the Manager, Site Contracts, in the day to day running of ...Notes are only visible to you.
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Clinical Safety Specialist
Novartis Pharmaceuticals (Singapore)
3. Ensure recording and tracking of receipts, submissions and distributions of SAEs, SUSAR, SRs, and Investigator Notification (IN). 4. Manage reporting/submission/distribution of safety reports/updates ... field forces, trial monitors and third party contractors, if applicable; oversee training to ...Notes are only visible to you.
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Sr Medical Science Liaison
Biogen Idec (Singapore)
based conduit for the receipt of proposals and subsequent communications related to Biogen-Idec funded Investigator Initiated Trials (IITs). Assist with communications related to Biogen Idec sponsored MSLs may be involved with site initiation, communication & coordination ...Notes are only visible to you.
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Clinical Research Associate (Early Phase - I/II)
Covance (Singapore)
proposal generation and feasibility tasks. . May participate in identification and recruitment of investigators, collection of investigator documentation, pre-study qualification visits and site management responsibilities. . Organizes and delivers presentations at Sponsor and Investigator/Initiation Meetings. . ...Notes are only visible to you.
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Senior Clinical Research Associate (CPS)
PAREXEL International LLC (Singapore)
sites have adequate time and can fulfill their obligation to the study. ¿ If appropriate, collect investigator site regulatory documents and perform Quality Check prior to submission to EC, Regulatory ... adhering to the protocol and address any ...Notes are only visible to you.
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Senior Clinical Research Associate
Abbott (Singapore)
D Shift Days Relocation Assistance Within Country Job Description .Conduct site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 ... Abbott Standard Operating Procedures (SOPs) and business processes. .Conduct all clinical ...Notes are only visible to you.
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Senior GCP Auditor
PAREXEL International LLC (Singapore)
Quality Assurance (Research Regulatory compliance) groups Travel to perform audits (e.g Investigator Site audits) Use in-depth understanding of appropriate GCP compliance and other applicable laws to provide guidance to PAREXEL and our clients regarding ...Notes are only visible to you.
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Associate Global Medical/Scientific Director Virology
Abbott (Singapore)
data. Specifically, responsible for strategy, planning, and execution of phase IIIb/IV studies, investigator initiated studies, registries, database analysis, and HEOR studies. Also responsible ... responsibility Percent of Travel 20 - 50 % Country Singapore State/Province Singapore ...Notes are only visible to you.
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Project Manager II - Oncology
INC Research (Singapore)
Customer proposal defense meetings. OTHER RESPONSIBILITIES: 1.• May perform or oversee site feasibility assessments. 2.• May participate in proposal and investigator grant determination. 3.• May participate in Customer proposal development. 4 ...Notes are only visible to you.
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