Clinical Project Manager

On behalf of our client, an international pharmaceutical, clinical stage drug discovery company, we are currently recruiting for a Clinical Trial Project Manager for the area of rare diseases. This is a 6-9 month contract initially. The role will be predominately based in the Dublin office with approx 5% travel.

Main Duties / Responsibilities:

The successful candidate will be required to manage multiple clinical sites in the US and Canada to GCP standards as well as trial vendors.

* They will be responsible for delivering all tasks and projects in a timely manner within budget taking a proactive approach at all times.
* They would also be expected to manage and monitor/audit clinical sites and related vendors onsite.
* Carry out various other additional tasks that may be required from time to time in accordance with the overall goals of the company

Requirements:

* Relevant Scientific degree with at least 4-5 years’ working in Clinical Research in a Phase I, II CRO and/or pharmaceutical company. (c.3 years as a CRA and c.2 years as a Clinical PM).
* GCP experience in the pharmaceutical industry
* Monitoring and project management experience
* A willingness to deal with international teams working in different time zones
* Therapeutic experience and scientific knowledge in rare disease is a distinct advantage.
* A flair for scientific writing (protocols and reports) and fully conversant with the use of EDC in clinical trials
* Excellent interpersonal, communication and problem solving skills
* Flexible in reacting to changing priorities in projects without compromising timelines and/or quality
* Ability to travel (domestic and international) as required

The position will be located in the Dublin office and salary will be based on level of experience

For full details contact Linda at +353 1 2784701 or email your CV to [email protected]. Thornshaw Scientific is a division of the CPL Group www.thornshaw.com