ere to Good Clinical Practice Standards at all times
Demands
and working after hours may be required from time to time TO APPLY:
record anatomical images, physical data and real time physiological information for health research purposes the research team to deliver the project goals on time and on budget Work with medical professionals to tact, and discretion must be maintained at all times Ability to manage self and prioritize own workload Self-motivated, able to work independently and work as part of a multidisciplinary team Ability to work under
record anatomical images, physical data and real time physiological information for health research purposes the research team to deliver the project goals on time and on budget Work with medical professionals to tact, and discretion must be maintained at all times Ability to manage self and prioritize own workload Self-motivated, able to work independently and work as part of a multidisciplinary team Ability to work under
Adhere to Good Clinical Practice Standards at all times Address relevant concerns about the study with participants projects, while maintaining independency and work as part of a multi-disciplinary team Demands of the job: and working after hours may be required from time to time TO APPLY: Only if you do meet the minimum job
Adhere to Good Clinical Practice Standards at all times Address relevant concerns about the study with participants projects, while maintaining independency and work as part of a multi-disciplinary team Demands of the job: and working after hours may be required from time to time TO APPLY: Only if you do meet the minimum job
special projects and duties as assigned from time to time. Kindly be advised that should you not receive
special projects and duties as assigned from time to time. Kindly be advised that should you not receive
Reports (PSURs/DSURs), as applicable, Plan and ensure timely submission of Aggregate Reports according to local Support LSO/CSTL in the preparation, conduct and timely documentation of Pharmacovigilance training for contributions and data, as needed, accurately and in a timely manner. Responsible for the local PSMF implementation
Reports (PSURs/DSURs), as applicable, Plan and ensure timely submission of Aggregate Reports according to local Support LSO/CSTL in the preparation, conduct and timely documentation of Pharmacovigilance training for contributions and data, as needed, accurately and in a timely manner. Responsible for the local PSMF implementation
research studies