My client a Cork based Pharma company require a Clinical Trial Scientist
Do you enjoy working as part or a problem solving collaborative team ?
Are you focused in healping patients access life saving treatments ?
This role could be for you. Some requirements ! ( Not exhaustive ).
- Provides frontline clinical trial capabilities in support of clinical development.
- Create & maintain contracts templates, process documentation & contract-specific documentation.
- Act as a mentor junior staff providing guidance & knowledge transfer enabling them to be successful negotiators.
- The Associate also provides clinical trial contract guidance to other Lilly business partners, including:
- Responsible for ensuring sites meet requirements into clinical trials (CT's) & support activities.
- You will be central in obtaining CT authorisation & ethical approvals.
- Central role in execution of the budget & contract & oversees inspection readiness
- Confortable in record keeping i.e "Master File" and collaboration with colleagues
- Ensures country specific regulatory & data privacy reqs are incorporated into submissions.
- You will have a basic understanding of legal & financial requirements.
- Passionate about shared learning & "continious improvement".
What you will need !
- Passionate about patient health and expereince in a regulated setting
- Contract negotiation expertise.
- Related Technical Degree with at least 2 years experience in clinical trials/research.
- Expereince with Master data filing or a related GDP platform.
- A solid understanding of clinical trial development.
- Fluency in a 2nd European language essential. Dutch/German/Romanian.French etc..
- Must enjoy working in a team. Project management skills
Interested ? Don't delay..talk to me today please.
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