Junior Clinical Research Associate (m/w/d), Single Sponsor
at IQVIA
Home Office, Tirol, Austria -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 23 Jan, 2025 | Not Specified | 24 Oct, 2024 | N/A | Life Science,Harmonization,Communication Skills,English,Regulatory Requirements,German | 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 |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
When you join IQVIA as a sponsor-dedicated Junior Clinical Research Associate / CRA (m/w/d) office-based in Vienna or home-based throughout Austria, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you’re just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
QUALIFICATIONS:
- University Degree in life science or other scientific discipline or apprenticeship in the health care field
- Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
- Fluency in German on at least C1 level and a good command of English
- Flexibility to travel up to 40-60% of working time
- Driver’s license class B
Responsibilities:
- Performing site selection, initiation, monitoring and close-out visits
- Supporting the development of a subject recruitment plan
- Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborating with experts at study sites and with client representatives
- Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices)
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
The health care field
Proficient
1
Home Office, Austria