QA/QC Professional/Associate Scientist, Contract, Switzerland

We have an exclusive long term contract role available to work onsite with a renowned Global Pharmaceutical company in Basel, Switzerland. This particular Global Pharmaceutical company is looking for a Trial Master File (TMF) Quality Control Manager for the end-to-end Quality Control of essential TMF documents for assigned trials/programs according to established timelines.As a QA/QC Professional you will be the single Point of Contact to the Therapeutic Areas (TA)/Clinical Trial Team (CTT) for TMF related questions and will oversight of TMF Quality Control Specialists.

Please see below for the minimum requirements of the role:

EDUCATION (minimum/desirable):

Bachelor's degree in life science/healthcare is required with minimum 4 years' experience in clinical operations and/or clinical systems management

or

Associate degree required with minimum 6 years' experience in clinical operations and/or clinical systems management

LANGUAGES:

Fluent English (oral and written)

EXPERIENCE/PROFESSIONAL REQUIREMENT:

- Experience in cross-functional, multicultural and international clinical trial teams; able to work independently.
- Ability to lead globally distributed matrixed teams
- Good knowledge of clinical development process, regulatory requirements and GCP.
- Excellent understanding of system data structures and Clinical Document Management System functionality
- Ability to learn new systems readily
- Strong computer skills (EXCEL, MS Word) required

We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract; alternative market rates are also welcome.

Please note there is a job description available on request.

We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will endeavour to get back to you with further information on the role and answer any questions you may have.

Kind regards,

Neha Sharma

Michael Bailey Associates

Job code: 109724

Key words: QA, QC, Quality assurance, quality control, Trial Master file, TMF, global trials, clinical trials, GCP, regulatory affairs, clinical development, data structures, clinical document management systems, clinical operations, SOP, subject matter expert, training, CTT, Switzerland, English.

Michael Bailey International is acting as an Employment Business in relation to this vacancy.