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Salary: On Application
for obtaining and maintaining regulatory authorisation for new products throughout Europe. You will project manage Market Authorization Applications from submission stage onwards, ensure that timelines are met for bringing new products
Requirements: authorisation for new products throughout Europe.
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This is an influential role with a successful and expanding global CRO. You will manage the global contracts team in the development, review and execution of contracts with Clinical Investigators and Institutions according to national and international law as well as internal and sponsor performance standards. Other responsibilities will include the maintenance of a library of country specific tem
Requirements: You will manage the global contracts team in the development, review and execution of contracts with Clinical Investigators and Institutions according to national and international law as well as internal and sponsor performance standards. Other responsib
Jobs similar to "rsa executive search new": rsa executive search new director
This global pharmaceutical company specializes in the development, production and marketing of both generic and proprietary branded pharmaceuticals. It is in fact one of the top 20 pharmaceutical companies and among the largest generic pharmaceutical businesses in the world. With strong development and growth plans they are looking to recruit a Pipeline Portfolio Manager to work closely with the H
Requirements: You will lead and co-ordinate the UK pipeline and provide a clear view on risk and opportunities, while ensuring that both UK and EU projects are delivered on or ahead of time.
Jobs similar to "rsa executive search new": rsa executive search new manager
Our client is an International Pharmaceutical group. They currently have a requirement for a QP within their Quality team. Duties To perform the duties of a Qualified Person in line with MHRA requirements to enable the release of products on a daily To review all batch related production and QC data To ensure current Good Manufacturing Practices To review and approve all other non batch related da
Requirements: Our client is an International Pharmaceutical group. They currently have a requirement for a QP within their Quality team.
Our client is a fast growing biopharmaceutical company based in Switzerland. Job Role and Responsibilities: Co-ordinate and oversee the validation aspects of projects, including Equipment Qualification; Computer Validation; Cleaning Validation and Process Validation Ensure that validation activities carried out by contractors complies with relevant cGMP standards, regulatory requirements, corporat
Requirements: Our client is a fast growing biopharmaceutical company based in Switzerland.
Management and Clinical Supplies to develop a study timeline and budget. This new development centre is testament of our client's commitment to develop an optimal structure for its global clinical development operations. The Clinical... Study Manager will be an integral member of this new team. This is an opportunity not to be missed. Educated to a minimum of a first science degree, you will demonstrate an excellent clinical research background with 4 - 5 years
Requirements: Our client, a global pharmaceutical organisation, is looking for a Clinical Study Manager to join them in the execution of Phase I-IV clinical R&D activities relating to the Asia Pacific Region. Based in Singapore and reporting to the Clinical Programme M
Responsibilitles To oversee the set-up and ongoing management of new projects to ensure that the client's requirements are being met and that company staff are assigned specific duties. This will include the following... of contact for the Sponsor company and to report to them as required To report to Steering Committees and National Co-ordinators as specified by the Sponsor company To be involved in the selection of new or assignment of existing
Requirements: To oversee the set-up and ongoing management of new projects to ensure that the client's requirements are being met and that company staff are assigned specific duties etc.
Excellent opportunity for Clinical Research Associates (CRA I, II, Senior). Our client is looking for experienced Clinical Research Associates. Job functions will include: Assist in the set-up of trials which may involve undertaking training by the Sponsor company Assist, if required, with the design of specific trial materials Ensure that the contractual documents between the centres, Sponsor com
Requirements: Excellent opportunity for Clinical Research Associates (CRA I, II, Senior). Our client is looking for experienced Clinical Research Associates.
For our client, a global pharmaceutical / biotech company we are looking for an international Public Policy Manager. This is a global role which allows the ideal candidate to identify policy barriers from governments/health authorities. She/He will handle the advocacy of patients group and will be responsible for training those groups. Responsibilities Works with pan-European and regional patient
Requirements: For our client, a global pharmaceutical / biotech company we are looking for an international Public Policy Manager. This is a global role which allows the ideal candidate to identify policy barriers from governments/health authorities. She/He will handle
Home-based
Company: RSA Executive Search NewSalary: On Application
This role is with a rapidly expanding global Clinical Research Organisation who require an experienced CRA to support Oncology trials. Assist in the set up of trials which may involve undertaking training by the Sponsor company Assist, if required, with the design of specific trial materials Ensure that the contractual documents between the centres, Sponsor companies and/or our Company are complet
Requirements: This role is with a rapidly expanding global Clinical Research Organisation who require an experienced CRA to support Oncology trials.