Job Designation: Drug Safety Associate - Pharmacovigilance Call Center Experience: Freshers Location: Hyderabad Email: Hr@jeevanscientific…
By: Jeevan
Science graduates with 0-3 years of experience in pharmaceutical research. Freshers Life science graduates 2019,2020,2021 passed out candidates will be…
By: Renovate Biologicals
Provides medical expertise for site identification, study feasibility, study design, conduct, analysis and reporting, generation of integrated databases, pooled…
By: QED Pharmaceutical Services
Hyderabad 0 to 3 years Full Time. Graduate/Post Graduate/Doctorate degree in Life Sciences/Pharmacy/Medical Sciences or equivalent degree.
By: Advity Research
Hyderabad 2 to 4 years Full Time. Graduate/Post Graduate/Doctorate degree in Life Sciences/Pharmacy/Medical Sciences or equivalent degree.
By: Advity Research
2-3 yrs experience in eCTD and SPL Publishing. Years of Experience 2-3 years Education Qualification for the position Any Degree…
By: Aurobindo Pharma USA Inc.
Lead External Suppliers Qualification process. Provide the quality presence and in-put to Technical meetings with the External suppliers and establish good…
By: Novartis
Through the partnership with more than 1000 external suppliers, our network of 7 technology platforms provides our customers and patients in more than 150…
By: Novartis
The candidate should have Bachelor’s Degree/Diploma in Pharmacy in the relevant branch with First Class or equivalent.
By: Narsee Monjee Institute of Management Studies (NMIMS)
High-level, strategic, and scientific role that involves developing, coordinating, and executing cutting-edge, effective, and efficient real world evidence…
By: Sanofi
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of…
By: Novartis
Responsible to ensure the efficacy of the document generated by the analysts in a compliant manner and ensure the ready availability of documents during audits.
By: Neuland Laboratories Ltd
Bacholer of Dental Surgery or full time post-graduate qualification in any discipline of medicine. Therapeutic Area Lead/Director Medical Affairs.
By: Dr.Reddy's
Master’s or Bachelor’s degree in Science / Pharmacy. At least 7-10 years’ experience in similar function in pharmaceutical industry.
By: PharmSol
Hyderabad 3 to 5 years Full Time. Graduate/Post Graduate/Doctorate degree in Life Sciences/Pharmacy/Medical Sciences or equivalent degree.
By: Advity Research
Master’s or Bachelor’s degree in Science / Pharmacy. At least 5 years’ experience in similar function in pharmaceutical industry (Especially Finished dosage…
By: PharmSol
Science graduates with 0-3 years of experience in pharmaceutical regulatory affairs. Freshers Life science graduates 2019,2020,2021 passed out candidates will…
By: Renovate Biologicals
Communication skills – written, verbal and listening. Pride in getting work done accurately and timely. Ability to make presentations to potential customers.
By: Multicure Pharma
Provide support as a team member of Analytical R&D – responsible for Analytical development works. Provide support in the Analytical development department, and…
By: Granules India
The role works on projects supporting existing and new products and/or new technologies under supervision from senior scientist, principal scientist or line…
By: Ferring Pharmaceuticals, Inc.
The role holder shall report to Lead – Process Research and shall perform research activities as designing and conducting scientific experiments, analysing and…
By: PI Industries Ltd.
To develop Intermediates/API orbio-pharma related business across all over India and abroad. To carry out all activities related toMarketing of Intermediates…
By: Pharmaceutical industry
Qualification - Masters in Science, M-Pharma, Pharm-D, MBBS, BDS, MSc, B. Excellent Subject Knowledge - Health Science, Pharmacology and Medical Science.
By: Infocusrx, Inc.
The responsibility of a CRA II is to perform all clinical monitoring/ site management activities for assigned projects in accordance with AXIS SOPs.
By: AXIS Clinicals
The Clinical Data Manager is responsible for overseeing all data management activities pertaining to the conduct of Phase I-IV clinical trials in accordance…
By: QED Pharmaceutical Services