EUROPEAN PHARMACEUTICAL STUDENTS’ ASSOCIATION IMP TRAINING PLACEMENT OFFER PARTNER Asphalion Asphalion is an International Drug Development and Regulatory Affairs Consultancy based in Barcelona. The firm is structured into working groups for International Registra- tion Procedures, Clinical and Medical Writing, Electronic Submission of Regulatory Data, CMC/Quality and Pharmacovigilance. www.asphalion.com Name Description Web PLACEMENT Description Name Area Regulatory Affairs Officer Regulatory Affairs • Preparation, elaboration, and revision of registration dossiers; presentation of those to Health Agencies and/or Organisms and management of all related documents. • Preparation of regulatory strategy dossiers or reports. • Evaluation and revision of non-clinical and quality documentation; participation in drug development programs, in collaboration with R&D and CRO groups. • Communication with international agents for regulatory support. Location Barcelona, Spain Duration 6 months (flexible start) Salary Salary according to experience and added value Mandatory Qualifications • University degree in Pharmacy, Chemistry, Biology or Medicine. • Fluent in English required. Knowledge of Spanish or other languages highly valued. • Experience will be valued with same functions in the registration field of human or veterinary medicines, APIs, medical devices or similar will be valued. Reception Logistics* handled by the National IMP Coordinator *Accommodation, VISA arrangements, Health Insurance, etc. APPLICATION Deadline More Info 15 th of October 2013 • [email protected] | Vice-President of Mobility | Rita Figueira • [email protected] | Central IMP Coordinator | Sonia Colianni

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EUR

EAN

CEU

TIC

STU

DEN

TS’ A

IATI

IMP TRAINING PLACEMENT OFFER

PARTNER

Asphalion

Asphalion is an International Drug Development and Regulatory Affairs Consultancy based in Barcelona. The firm is structured into working groups for International Registra-tion Procedures, Clinical and Medical Writing, Electronic Submission of Regulatory Data, CMC/Quality and Pharmacovigilance.

www.asphalion.com

Name

Description

Web

PLACEMENT

Description

Name

Area

Regulatory Affairs Officer

Regulatory Affairs

• Preparation, elaboration, and revision of registration dossiers; presentation of those to Health Agencies and/or Organisms and management of all related documents.

• Preparation of regulatory strategy dossiers or reports.• Evaluation and revision of non-clinical and quality documentation; participation in

drug development programs, in collaboration with R&D and CRO groups. • Communication with international agents for regulatory support.

Location Barcelona, Spain

Duration 6 months (flexible start)

Salary Salary according to experience and added value

MandatoryQualifications

• University degree in Pharmacy, Chemistry, Biology or Medicine.• Fluent in English required. Knowledge of Spanish or other languages highly valued.• Experience will be valued with same functions in the registration field of human or

veterinary medicines, APIs, medical devices or similar will be valued.

Reception Logistics* handled by the National IMP Coordinator*Accommodation, VISA arrangements, Health Insurance, etc.

APPLICATION

Deadline

More Info

15th of October 2013• [email protected] | Vice-President of Mobility | Rita Figueira• [email protected] | Central IMP Coordinator | Sonia Colianni