Opening For Regulatory Affairs Specialist At Pra Health Sciences

Opening For Regulatory Affairs Specialist At Pra Health Sciences
Opening For Regulatory Affairs Specialist At Pra Health Sciences
Hiring an Associate level Regulatory Publishing Specialist with 1 to 3 years experience in the industry and preferably having exposure to regulatory submissions in other regions outside of APAC. PRA India can offer you a lucrative career in this space with many opportunities for internal progression pathways as the business and our global client base keeps on growing. If you'd like to hear more about this role which is home-based anywhere in India, please send cv on today: MalvankarShambhavi@prahs.com



Comments

Post a Comment

Popular posts from this blog

Opening For Clinical Research Associate At Sun Pharma

Image
Opening For Clinical Research Associate At Sun Pharma Opportunity to work as CRA (Site Ahmedabad / Baroda) - Sun Pharma R&D Qualification: B. Pharm with PG diploma in Clinical Research/ M. Pharm / Masters in Clinical Research. Experience: Experience: 2-3 years of experience in Clinical Research / Bioavailability & Bioequivalence Studies / CRA / CRC JD: 1. Monitoring of outsourced bioavailability & bioequivalence studies Good Clinical Practices (GCP), Good Laboratory Practices ( 2. To perform Site Selection Visits, Site Initiation Visit, Site Monitoring Visit and Site Closeout Visit for patient based outsourced pharmacokinetic studies. 3. Review E-CRFs and electronically captured source data. 4. Verify the Trial Master Files for content and completeness at the clinical/investigator sites and manage/maintain the Trial Master Files for the sponsor. 5. Co-ordinate with Sponsor and CROS/Investigator sites for study monitoring activities and updates. Send in your resume to: Rosem...
Read more