Sr Cra

Hobson Prior are seeking for a SR CRA to join a brilliant CRO on a permanent basis located anywhere in Germany with the ability to travel within the DACH region. Our client is focused on personalised and scalable solutions.

Please note that to be considered for this role you must have the right to work in this location.

**Key Responsibilities**:

- For this position, you will be accountable for gathering and examining necessary documents and conduct reconciliation of investigator site file.
- Attend both internal and external project calls as requested and per budget to actively offer necessary site updates.
- You will examine IP responsibility, dispensation as well as compliance at the investigative sites.
- Perform pre-study visits, site initiation visits site supervising visits and site closeout visits per SOPs/WPDs.
- Any other assigned duties.

**Key Skills**:

- Able to make decisions on an independent basis with the ability to resolve issues.
- Presentation abilities.
- Communication skills both verbally and in writing.
- A motivated individual with the ability to train others.

**Requirements**:

- Educated to a degree level in a nursing, life science, or medical science discipline or comparable work experience.
- Familiarity in a clinical research associate role with exhibited ability in clinical research fundamentals.
- Acquaintance with CTMS, eTMF IXRS and EDC systems.
- Prior involvement working within a CRO.
- Fluency in the English language with knowledge in the host country language.
- Expertise on regional clinical research guidelines and ICH-GCP.
- Familiarity with various therapeutics with the ability to obtain in-depth protocol expertise.
- Capable of forming/upholding relationships with sites/associates/clients.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.