DS Biopharma is always interested in hearing from applicants with experience in CMC, clinical research and regulatory affairs.  Please feel free to send your curriculum vitae to DS Biopharma via info@dsbiopharma.com and we will contact qualified applicants when positions become available.

We currently have the following vacancy:

 

Clinical Trial Projects Manager

Main Duties / Responsibilities:

The successful candidate will be required to manage multiple clinical projects to GCP standards. They will provide oversight of all the responsibilities transferred by DS to CROs and other 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 both CROs 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 as a CRA and then CPM.
  • 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 Dermatology 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 Leopardstown, Dublin, Ireland office.
Applications can be sent to info@dsbiopharma.com

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