Search Results: 4,845 vacancies
Job Description
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those...
Rs 10 - 13 lakhs p.a.
...incl. charts and graphs, smart arts etc
Pharma Healthcare, Secondary Research, Scientific writing, OTC, Rx ,OTC Pharma Healtcare,Consumer Pharma Healthcare
Designation: CDMA | Clinical Development Medical Affairs
Vacancies: 5
Experience: 5.0 Year(s) - 7.0 Year(s)...
...Job Title: Regulatory Affairs Analyst Location: Bangalore
Job Type: Full-time
Years of Experience: 2-5
Company Description:... ...mortality rates. Origin Medical is headquartered in Singapore with clinical research teams located in India and Vietnam.
About the team...
...to make life better for people around the world.
Job summary
The MAP is a therapeutically aligned Clinical Scientist who plays a key role within the Medical Affairs organization. The primary focus of this role is to use the individual’s knowledge of specific disease...
...activities related to CTA submissions in IM
- Create a database of clinical requirements for CTA submission in IM
- Work closely with... ...field
- At least 5 years of experience in regulatory affairs for pharmaceuticals/biologics (or equivalent combination of regulatory...
...dossiers in the format of CTD/ACTD.
Check the compliance status of the Quality Systems.
Evaluate and comment on requirements of Clinical studies.
Prepare artwork of packaging materials as per current rules and regulations.
Must have worked on ASEAN, CIS, and...
...coordination with different SBU/Divisional heads
Providing medical/clinical oversight regarding positioning strategy and implementation... ...Engagement of identified key scientific leaders through medical affairs activities, in alignment with the overall franchise plan and...
...regulatory requirements to product development teams
Advises stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations
Assesses the acceptability of quality, preclinical, and clinical document for submission...
...and medical education? We are looking for a Director - Medical Affairs and Medical Education to join our team at Novo Nordisk. If you are... ...in cross-functional teams.
About the department
The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...
...Regulatory Affairs Specialist
Responsibilities:
Prepare and submit regulatory documentation for new and existing medical products... ...their inquiries.
Manage the regulatory approval process from pre-clinical development to post-market surveillance.
Develop and...
...best internal and external benchmarks
What you will do
The Clinical Evaluation Specialist acts as the lead technical expert in... ...experience (PhD, Post-doc)
Experience in clinical or regulatory affairs preferred
Experience with orthopedic or trauma devices preferred...
...increasingly complex and stressed health system, Lilly Medical Affairs (MA) can provide clear, credible answers that will set Lilly apart... ...payers and focuses on answering HCP questions with customized clinical and real-world evidence that can make the difference on if and how...
...Description :
Job Title:
Ideation Specialist (Medical Affairs)
Job Category:
Head Office Based Medical Affairs... ...Experience:
Medical Qualification:0-2 years of experience in clinical development, R & D or medical affairs
Pharmacy Qualification:...
...opportunities arising from the intersection of statue and regulation with clinical development decisions and product profiles.
The Opportunity:... ...You are someone with a 10+ years of experience in Government Affairs, of which at least 5 years should be in a Multinational Company....
Position Overview: - We are seeking a skilled Policy and State Government Associate to join our dynamic team. The ideal candidate will have a minimum of 7-9 years of experience in either project management at a political/government consulting firm or policy experience in an...
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working... ..., including project teams, clinical operations, and regulatory affairs. Foster collaborative relationships with external stakeholders,...
Client's Company Profile:
Our client is into Import & Export of Pharmaceutical / Medical Device Company (European MNC). The company provides tailored intelligent healthcare solutions based on the latest professional insights, and on decades of experience in Africa.
They...
...Job Description
Job TitleAssociate Director Regulatory Affairs MoSJob Description Associate Director Regulatory Affairs MoS
Critical... ...functional category leadership team (e.g., Marketing, R&D, Clinical, Quality) to understand patient and market needs and developing...
...~ Time management
Presentation skills .
Interpersonal skills.
Experience-- 4-5 Years of Experience in Pharma Regulatory Affairs
Job Summary
Core understanding of technical requirements in the CTD
Coordinate with Plant and associated departments to facilitate...
...Description
Department : DIT, IB & MAPA & Corp Com
Location : Bangalore
Can you implement, manage and drive country-wide Public Affairs strategies at central Govt. level and at state Govt. level? Do you have the interpersonal skills to navigate in a complex stakeholder...
