Job Description
1. To support the ongoing clinical trial application project.
2. To support all regulatory activities based on project requirement.
1. To support the ongoing clinical trial application project.
2. To support all regulatory activities based on project requirement.
Candidate Profile
1) A master degree in a relevant educational field - life science, pharmacy, others.
2) 0 to 6 months experience with Pharmaceutical industry or CRO with general understanding of Regulatory Affairs.
3) Good communication skills, quick learner and computer savvy.
4) Willing to work preferably in EU shift or as per project requirement
1) A master degree in a relevant educational field - life science, pharmacy, others.
2) 0 to 6 months experience with Pharmaceutical industry or CRO with general understanding of Regulatory Affairs.
3) Good communication skills, quick learner and computer savvy.
4) Willing to work preferably in EU shift or as per project requirement
Additional Information:
Location: Bengaluru, Karnataka, India
Education: M.Pharm, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Regulatory Affairs
End Date: 20th February, 2019
Location: Bengaluru, Karnataka, India
Education: M.Pharm, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Regulatory Affairs
End Date: 20th February, 2019
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