(Senior) Clinical Trial Associate*
at Immatics Biotechnologies GmbH
72076 Tübingen, Baden-Württemberg, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 15 Sep, 2024 | Not Specified | 17 Jun, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
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Contract to Hire – Corp 2 Corp |
Description:
OVERVIEW
We are currently seeking a (Senior) Clinical Trial Associate* to strengthen our Clinical Operations department. You will work in an interdisciplinary environment with colleagues from Germany and Houston (TX, USA). Your analytical reasoning and action-oriented style as well as your organization and communication skills will contribute to the team’s success. The position can be located in Tübingen, Munich or remote (in Germany).
ABOUT US
Immatics combines the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors with the goal of enabling a robust and specific T cell response against these targets. This deep know-how is the foundation for our pipeline of Adoptive Cell Therapies and TCR Bispecifics as well as our partnerships with global leaders in the pharmaceutical industry. Operating from Tuebingen, Munich and Houston, we are committed to delivering the power of T cells and to unlocking new avenues for patients in their fight against cancer. For more detailed information, visit www.immatics.com.
Responsibilities:
- Providing support for GCP compliant clinical trial planning, conducting and overseeing clinical trials
- Keeping oversight, incl. but not limited to:
- tracking tools set-up and maintenance
- clinical trial documents preparation, review and/ or quality control
- Providing support to the administration of clinical trials based on the oversight, incl. but not limited to:
- meeting organization
- preparation of meeting minutes
- coordination of review processes and signature retrieval
- preparation of the Investigator Site File template
- print/ arrange printing service
- collection of essential site documents and eTMF upload
- Organizing investigator grant payments with global oversight of investigator grant payments
- Supporting development and maintenance of SOPs, guidance documents & training materia
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
72076 Tübingen, Germany