Senior Clinical Research Associate, Sponsor-dedicated
at IQVIA
távmunka, , Hungary -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 06 Nov, 2024 | Not Specified | 08 Aug, 2024 | 2 year(s) or above | Time Management,Computer Skills,Regulatory Requirements | 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:
SENIOR CLINICAL RESEARCH ASSOCIATE
IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.
When you join IQVIA Zagreb as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
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 scientific discipline or health care
- At least 2 years of on-site monitoring experience
- Good knowledge of clinical research regulatory requirements
- Very good computer skills including MS Office
- Excellent command of Croatian and English language
- Organizational, time management and problem-solving skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Flexibility to travel
- 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
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Scientific discipline or health care
Proficient
1
távmunka, Hungary