Accountancy
118
Agriculture, Fishing
1
Finance, Insurance
95
Call Centres
0
Catering & Hospitality
102
Construction, Property
127
Customer services
59
Defence/Armed Forces
67
Education
2
Electronics
76
Engineering, Manufacturing 121
Graduate, Trainees
67
Healthcare & Nursing
60
Human resources
79
IT & Internet
534
Legal
69
Management consultancy 70
Marketing, Advertising, PR 88
Media, Creative
8
Non-profit, Charities
0
Public sector & Services
10
Recruitment sales
64
Retail, Wholesale
61
Restaurant & Food Service 5
Sales
134
Science
12
Secretarial, Administration 17
Security
0
Senior appointments
10
Telecommunications
3
Transport, Logistics
5
Travel, Leisure, Tourism
26
Other
73
| |
Accountancy
0
Agriculture, Fishing
0
Finance, Insurance
0
Call Centres
0
Catering & Hospitality
0
Construction, Property
0
Customer services
0
Defence/Armed Forces
0
Education
0
Electronics
0
Engineering, Manufacturing 0
Graduate, Trainees
0
Healthcare & Nursing
0
Human resources
0
IT & Internet
0
Legal
0
Management consultancy 0
Marketing, Advertising, PR 0
Media, Creative
0
Non-profit, Charities
0
Public sector & Services
0
Recruitment sales
0
Retail, Wholesale
0
Restaurant & Food Service 0
Sales
0
Science
0
Secretarial, Administration 0
Security
0
Senior appointments
0
Telecommunications
0
Transport, Logistics
0
Travel, Leisure, Tourism
0
Other
0
| |
|
|
Section: Science Vacancy 914 |
| Post:Pharmacovigilance Co-Ordinator I
|
Salary contractual |
| |
| Requirements and conditions |
| Age: |
Has no value
|
| Gender |
Has no value
|
| Education: |
no
|
| Work schedule: |
Has no value
|
| Work place: |
Sheffield
|
| The announcement text: |
We are assisting this CRO in their bid to recruit a Pharmacovigilance Co-ordinator I. The successful job holder will be responsible for the processing and reporting of safety information to the sponsor, affiliates, and for the development and maintenance of the SAE files and tracking systems.
The role:
• Processing & reporting of safety events
• Developing & maintaining the Safety Events tracking log system
• Developing & maintaining a working knowledge of assigned studies
• Participating in the preparation of relevant documents
• Ensuring compliance with relevant standards
• Participating in the process of developing & review of SOPs
• Maintaining a high level of expertise with client projects and marketplace developments
Experience:
• Relevant bachelor degree or equivalent clinical research experience
• Experience in pharmacovigilance, Clinical research or related field an advantage
• Ability to learn & apply SOP’s and FDA regulations pertaining to clinical studies
|
| Contact information |
| Employer: |
|
| Email: |
515@jobinleeds.informnow.com
|
| Phone: |
01252 811333
|
|
| |
Publication date: 2009-04-08 21:22:26
|
| |
|
|
