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Senior CRA 6 Month Contract - New Jersey
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Client
Projektbeschreibung
I have an excellent role that I am looking to fill that could be of interest to you.
My Client, based in the New Jersey, is looking for a Senior Clinical Research Associate to complete project activities associated with monitoring functions of Phase I-IV clinical research studies.
They will be performing investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs).
Responsibilities include:
- Perform study start-up activities related to monitoring activities
- Develop and implements innovative approaches for and participates in site recruitment, selection, and initiation activities
- Participates in CRA protocol specific training and development activities
- Develops and implements innovative approaches for the preparation and coordination of investigator meetings and participates in meeting
- Develops patient enrolment strategies with the project team and clinical trial sites
- Knowledge, Skills, and Abilities:
- Knowledge of FDA regulatory requirements (i.e. GCPs, CFRs, etc.)
- Education and Work Experience:
- Bachelor's Degree in allied health fields such as Nursing, Pharmacy, or Health Science, preferably with clinical trial monitoring experience
- Minimum of 2-3 years of clinical research monitoring experience
- Must be able to handle a workload of multiple protocols / multiple sites.
Rate: Market Rates
Location: New Jersey
Duration: 6 Months
If you are interested in this opportunity please forward your CV and I will get in contact with you ASAP.
To find out more about Real please visit www.realstaffing.com
My Client, based in the New Jersey, is looking for a Senior Clinical Research Associate to complete project activities associated with monitoring functions of Phase I-IV clinical research studies.
They will be performing investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs).
Responsibilities include:
- Perform study start-up activities related to monitoring activities
- Develop and implements innovative approaches for and participates in site recruitment, selection, and initiation activities
- Participates in CRA protocol specific training and development activities
- Develops and implements innovative approaches for the preparation and coordination of investigator meetings and participates in meeting
- Develops patient enrolment strategies with the project team and clinical trial sites
- Knowledge, Skills, and Abilities:
- Knowledge of FDA regulatory requirements (i.e. GCPs, CFRs, etc.)
- Education and Work Experience:
- Bachelor's Degree in allied health fields such as Nursing, Pharmacy, or Health Science, preferably with clinical trial monitoring experience
- Minimum of 2-3 years of clinical research monitoring experience
- Must be able to handle a workload of multiple protocols / multiple sites.
Rate: Market Rates
Location: New Jersey
Duration: 6 Months
If you are interested in this opportunity please forward your CV and I will get in contact with you ASAP.
To find out more about Real please visit www.realstaffing.com
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung