Senior Clinical Research Associate
Covance
-
Sydney,
AUS
Clinical Research
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
- Responsible for all aspects of site management as prescribed in the project plans
- General On-Site Monitoring Responsibilities:
o Ensure the study staff ... Read More
|
Senior Clinical Research Associate
Covance
-
Sydney,
AUS
Clinical Research
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
- Responsible for all aspects of site management as prescribed in the project plans
- General On-Site Monitoring Responsibilities:
o Ensure the study staff ... Read More
|
Specialist II, Global Site Services
Covance
-
Sydney,
AUS
Clinical Research
Job Description:
- Develop project specific plans for the GSS component of assigned studies
- Liaise with operational project team regarding project issues (i.e., participate in team meetings)
- Collect, review, approve process and track regulatory & investigator documents required for study site activation in accordance with Covance SOPs, sponsor SOPs, GCP ICH guidelines and the Investigator ... Read More
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Programmer I (Contract)
Covance
-
Sydney,
AUS
Other
Job Description:
- Ensure quality of personal work.
- Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics.
- Prioritize personal workload to meet specified completion dates.
- Display a positive attitude at all times, promoting and contributing to a good team spirit with a productive and professional environment.
- Develop good ... Read More
|
Senior Clinical Research Associate
Covance
-
Sydney,
AUS
Clinical Research
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
- Responsible for all aspects of site management as prescribed in the project plans
- General On-Site Monitoring Responsibilities:
o Ensure the study staff ... Read More
|