本文发表在 rolia.net 枫下论坛Senior Research Co-ordinator
The University of Toronto Maternal, Infant and Reproductive Health Research Unit (MIRU) is the Data and Clinical Co-ordinating Centre for several multicentre national and international clinical trials as well as other clinical research projects, evaluating clinical questions of importance to the health of women and their infants.
We are seeking a full-time Senior Research Co-ordinator. The successful applicant will be expected to assume responsibility for the day-to-day administration of a major international multicentre clinical trial, including study co-ordination, organisation of international collaborators meetings, supervision of project staff, management of the data, and statistical analyses as required.
Candidates should have a Master’s degree or the equivalent in work experience; a clinical professional degree (e.g. BScN) would be an asset. Experience in the co-ordination and management of national or international multicentre clinical trials is preferable. A thorough working knowledge of SAS, Microsoft Access, and Microsoft Word are essential. Expertise with Teleform and Quicken would be an asset. The successful applicant must have excellent leadership and interpersonal skills; be able to develop and maintain close working relationships with health professionals; be able to communicate easily and successfully, in English, both verbally and in writing; be able to remain calm under pressure and meet deadlines while paying meticulous attention to detail.
Deadline for applications:
Please apply in writing including a resume and references, to:
Judy Cardwell
Administrative Co-ordinator, MIRU
790 Bay Street, Suite 751
Toronto, ON M5G 1N8
Fax: 416-351-3771
Email: miru@sw.ca
Only applicants who are to be interviewed will be contacted by telephone.更多精彩文章及讨论，请光临枫下论坛 rolia.net
The University of Toronto Maternal, Infant and Reproductive Health Research Unit (MIRU) is the Data and Clinical Co-ordinating Centre for several multicentre national and international clinical trials as well as other clinical research projects, evaluating clinical questions of importance to the health of women and their infants.
We are seeking a full-time Senior Research Co-ordinator. The successful applicant will be expected to assume responsibility for the day-to-day administration of a major international multicentre clinical trial, including study co-ordination, organisation of international collaborators meetings, supervision of project staff, management of the data, and statistical analyses as required.
Candidates should have a Master’s degree or the equivalent in work experience; a clinical professional degree (e.g. BScN) would be an asset. Experience in the co-ordination and management of national or international multicentre clinical trials is preferable. A thorough working knowledge of SAS, Microsoft Access, and Microsoft Word are essential. Expertise with Teleform and Quicken would be an asset. The successful applicant must have excellent leadership and interpersonal skills; be able to develop and maintain close working relationships with health professionals; be able to communicate easily and successfully, in English, both verbally and in writing; be able to remain calm under pressure and meet deadlines while paying meticulous attention to detail.
Deadline for applications:
Please apply in writing including a resume and references, to:
Judy Cardwell
Administrative Co-ordinator, MIRU
790 Bay Street, Suite 751
Toronto, ON M5G 1N8
Fax: 416-351-3771
Email: miru@sw.ca
Only applicants who are to be interviewed will be contacted by telephone.更多精彩文章及讨论，请光临枫下论坛 rolia.net