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Associate Medical Director
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support, Design
Projektbeschreibung
Associate Medical Director wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Master degree or equivalent medical degree with 4+ years' of clinical practice experience is preferred
- 3+ years' of profound background in clinical research or drug development in an academic or industry environment as well as 2+ years' experience of contribution to and accomplishment in all aspects of conducting clinical trials
- Proficiency and clinical training in a medical/scientific area with Medical Board certification would be an advantage
- Know How of the assigned disease area is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trials or program levels
- Expertise in clinical practice, statistics, clinical trial design including regulatory and clinical development processes
- Familiarity with Microsoft Office Suite programs
- Languages: fluent English both written and spoken
YOUR TASKS:
- Performing clinical leadership, medical and scientific strategic input and contributing to development of trial related documents for assigned clinical trials consistent with Integrated Development Plan
- Developing materials for trial-related advisory boards, data monitoring committees, investigator meetings and protocol training meetings for the company's local medical organizations
- Providing medical and scientific input and contributing to clinical sections of trial and program level regulatory documents
- Guaranteeing direct medical support of trials and act as medical monitor as well as supervising ongoing medical and scientific review of clinical trial data with Clinical Scientific Experts
- Giving input into final analyses and interpretation including the development of the Clinical Study Report, publications and internal as well as external presentations
- Securing overall safety of the compound for assigned trials in collaboration with Patient Safety
START: ASAP
DURATION: 06MM+
LOCATION: Basel, Switzerland
REF.NR.: BH13552
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND?
In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
YOUR EXPERIENCE/SKILLS:
- Master degree or equivalent medical degree with 4+ years' of clinical practice experience is preferred
- 3+ years' of profound background in clinical research or drug development in an academic or industry environment as well as 2+ years' experience of contribution to and accomplishment in all aspects of conducting clinical trials
- Proficiency and clinical training in a medical/scientific area with Medical Board certification would be an advantage
- Know How of the assigned disease area is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trials or program levels
- Expertise in clinical practice, statistics, clinical trial design including regulatory and clinical development processes
- Familiarity with Microsoft Office Suite programs
- Languages: fluent English both written and spoken
YOUR TASKS:
- Performing clinical leadership, medical and scientific strategic input and contributing to development of trial related documents for assigned clinical trials consistent with Integrated Development Plan
- Developing materials for trial-related advisory boards, data monitoring committees, investigator meetings and protocol training meetings for the company's local medical organizations
- Providing medical and scientific input and contributing to clinical sections of trial and program level regulatory documents
- Guaranteeing direct medical support of trials and act as medical monitor as well as supervising ongoing medical and scientific review of clinical trial data with Clinical Scientific Experts
- Giving input into final analyses and interpretation including the development of the Clinical Study Report, publications and internal as well as external presentations
- Securing overall safety of the compound for assigned trials in collaboration with Patient Safety
START: ASAP
DURATION: 06MM+
LOCATION: Basel, Switzerland
REF.NR.: BH13552
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND?
In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Sonstiges