Search Results: 70,442 vacancies
Rs 10 - 13 lakhs p.a.
...approval of Global promotional and awareness materials
Managing Promotional and Non-Promotional content approval process,... ...,Consumer Pharma Healthcare
Designation: CDMA | Clinical Development Medical Affairs
Vacancies: 5
Experience: 5.0 Year(s) - 7.0 Year(s)...
...countries around the world. We support pharmaceutical, biotechnology, and medical device companies with the services needed to perform clinical trials of new medicines. Our work helps patients in need improve their well-being – a fundamental driver for many of us to show up...
...Then read on!
We are currently seeking a Medial and Scientific Affairs Manager who will be responsible for supporting our global Medical and... ...scientific community, including key experts and customers in clinical and research laboratories, professional societies, government...
...needs to develop and/or disseminate the clinical and scientific evidence supporting key BSC... ...adoption through differentiated medical affairs efforts. The role will require travelling... ...trends in coronary interventions, rhythm management, electrophysiology, and structural heart...
...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...
...manufacturing & innovation space with the mission of enhancing peoples life globally for supporting their hiring requirement for Government Affairs Manager APAC Region.
Key Skills: Focus on the Person qualifications with the competencies to communicate/ influence effectively...
...Manager – Global Regulatory Affairs Location – Head-Office, Bangalore, IN
BIOCON BIOLOGICS
Biocon Biologics, we are creating a model for the... ...to end expertise from clone development, manufacturing, clinical development, regulatory approvals to commercialization in...
...Position : Clinical Data Manager Requirement: Immediate Joiner
Location : Hyderabad only
Experience: 5 to 10 Years only
Key Roles & Responsibilities:
Provide leadership and vision to the team.
Manage and deliver large-scale, high-complexity studies...
...expertise from clone development, manufacturing, clinical development, regulatory approvals to... ...and emerging markets. Global Regulatory Affairs
The Global Regulatory Affairs (GRA) at... ...; analytical sciences; quality management systems; regulatory writing and procedures...
...Medical Clinic Manager
Job Location: Mumbai, India.
Job Schedule: Part Time.
Job Type: 6 month contract to hire position.
Pay Rate: TBD.
Full Description:
VitalCheck Wellness is looking for a Medical Clinic Manager to work part time in an outpatient clinic...
...ROLE SUMMARY As part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management... ...timely and high-quality data review and query management of clinical data supporting the Pfizer portfolio. The Data Manager executes...
...Responsibilities:
Receive and process clinical trial documents, ensuring proper filing and... ...and best practices.
Track and manage document versions and ensure timely filing... ...associates, data managers, and regulatory affairs specialists.
Stay up-to-date on evolving...
...Partnership and Integrity. We want to be the Clinical Research Organisation that delivers... ...consistent deliverables for Global Scientific Affairs.
Maintain and configure testing and... ...relevant responsibilities as requested by management.
Recognize, exemplify and adhere to...
...strategic approach, policies, budget and creative direction of new events methods to transform the digital experience of company events
Manage communications and promotional materials for special events
Develop approach and methods to evaluate and measure event success....
...Regulatory Affairs Specialist
Responsibilities:
Prepare and submit regulatory documentation for new and existing... ...agencies and respond to their inquiries.
Manage the regulatory approval process from pre-clinical development to post-market surveillance.
Develop...
...data in Scientific advise from EU Agencies such as BfArM
Thorough knowledge of EU Variations in EU
Knowledge of the review of CMC/Clinical/Regulatory documentation required for submission
Working capabilitles preferably on PharmaReady or equivalent software
Working...
...Manage the overall general affairs function of the company and purchasing equipment and supplies.
Collaborate with external parties including, landlords, and service providers to establish and manage vendor relationships and contract negotiations.
Oversee the administrative...
...Glynase and more.
Responsibilities:
For the CMC RA position: Biosimilar Product Development Regulatory support – CMC
For the Clinical RA position Biosimilar Product Development Regulatory support - Clinical
Biosimilar Regulated market submissions - US / EU or US...
...Overview:
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below... ...and influenza including Harvoni and Sovaldi.
Position: Clinical Trials Manager
Location: Foster City CA 94404
Duration...
Manager of Medical Affairs - Ophthalmology
at Harrow, Inc.
(View all jobs)Remote
Before reading the job post, we encourage you to watch... .... We are data-driven and use our access to real-world clinical experience to lower the investment risks of our work. We concentrate...
