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Clinical Trial Manager
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Design, Support
Projektbeschreibung
Clinical Trial Manager wanted for one of our Basel based clients in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Degree or equivalent education in life science healthcare, PharmD, PhD is preferred
- 3+ years of technical and operational experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organization
- Extensive working experience in leading clinical trial, from feasibility to CSR
- Working experience in developing effective relationships with key investigators
- Excellent knowledge of good clinical practice, clinical trial design, statistics, regulatory processes, and global clinical development process
- Strong ability to work independently, lead a multidisciplinary trial team in a complex Matrix environment, knowledge of the Oncology and/or Hematology is of advantage
- Languages: fluent English both written and spoken
YOUR TASKS:
- Supporting the recording of clinical protocols and related documents in collaboration with the franchise medical directors and MSE besides managing clinical trial protocol development process
- Taking part in the development of effective working relationship with key investigators in assigned therapy area to optimize scientific quality/innovation of clinical study design, execution, reporting and publication
- Leading and supervising the global multidisciplinary CTT to ensure all trial deliverables are met according to timelines, budget, quality standards and operational procedures
- Contributing to the clinical trial data ongoing medical/scientific review, final analysis and interpretation as well as supporting the COM to develop clinical outsourcing specifications to facilitate bid templates and selection of CROs
- Predicting trial resource needs along with assisting COM in the development, management and tracking of trial budget, working closely with the appropriate groups in Oncology
- Supporting the development of clinical sections of regulatory documents like Investigators' Brochures, briefing books, safety updates, IND/NDA submission documents and responses to health authorities' questions
START: 01/2017
DURATION: 12MM++
LOCATION: Basel, Switzerland
REF.NR.: BH 9883
Does that sound interesting? Does that sound like a challenging opportunity to you? Then take the next step and send us your CV as a Word Document and a daytime 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:
- Degree or equivalent education in life science healthcare, PharmD, PhD is preferred
- 3+ years of technical and operational experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organization
- Extensive working experience in leading clinical trial, from feasibility to CSR
- Working experience in developing effective relationships with key investigators
- Excellent knowledge of good clinical practice, clinical trial design, statistics, regulatory processes, and global clinical development process
- Strong ability to work independently, lead a multidisciplinary trial team in a complex Matrix environment, knowledge of the Oncology and/or Hematology is of advantage
- Languages: fluent English both written and spoken
YOUR TASKS:
- Supporting the recording of clinical protocols and related documents in collaboration with the franchise medical directors and MSE besides managing clinical trial protocol development process
- Taking part in the development of effective working relationship with key investigators in assigned therapy area to optimize scientific quality/innovation of clinical study design, execution, reporting and publication
- Leading and supervising the global multidisciplinary CTT to ensure all trial deliverables are met according to timelines, budget, quality standards and operational procedures
- Contributing to the clinical trial data ongoing medical/scientific review, final analysis and interpretation as well as supporting the COM to develop clinical outsourcing specifications to facilitate bid templates and selection of CROs
- Predicting trial resource needs along with assisting COM in the development, management and tracking of trial budget, working closely with the appropriate groups in Oncology
- Supporting the development of clinical sections of regulatory documents like Investigators' Brochures, briefing books, safety updates, IND/NDA submission documents and responses to health authorities' questions
START: 01/2017
DURATION: 12MM++
LOCATION: Basel, Switzerland
REF.NR.: BH 9883
Does that sound interesting? Does that sound like a challenging opportunity to you? Then take the next step and send us your CV as a Word Document and a daytime 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
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Kategorie:
Medien/Design, Sonstiges