Locatie:
LEIDEN

Salaris indicatie:


Opleidingsniveau:
HBO

Werkzaamheden:
Responsibilities will include timely preparation and submission of correspondence and applications to regulatory agencies, tracking and planning of such and document conformance to global publishing standards.
- Ensure timely preparation and submission of correspondence and applications to regulatory agencies, tracking and planning of such and document conformance to global publishing standards and style manuals.
- Responsible for timelines and own resource management. Participates in extended teams/projects/teams. Ensures timely internal communication regarding regulatory filing status.
-Ensures compliance with Regulatory Agency rules and guidelines pertaining to regulatory submissions.

Profiel:
1-2 years
- BS /MS
- Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members.
- Good written and oral communication skills in English.
- High integrity with respect to maintenance of proprietary, confidential information.


Bedrijfsinformatie:
For an international pharmaceutical company in Leiden, we are looking for an Regulatory Operations Associate for 40 hours a week from 1/4 till 30/6. Do you have excellent communication and presentation skills in English? Send us your motivation and your CV in English to leiden238@adecco.nl

Interesse?
Stuur ons dan je CV en motivatie toe door te klikken op onderstaande knop "Reageer op deze vacature".