Regulatory Affairs on regulatory product landscape and strategies as a part of overall drugdevelopment strategy.
• Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts).
• Review...
impurities and contaminants in Drug Substances and Finished Products (Small molecules or Biologics) Development, qualification and validation of new analytical methods for the above activities Data interpretation Preparation of presentations and reports on...
As a Senior Scientist Nonclinical Safety and Drug Metabolism and Pharmacokinetics, you will provide support to ongoing and planned nonclinical programs at early and late stages of drugdevelopment.
This position is open to hybrid working...
High School and/or College Degree
• A significant experience in a similar job in the industry or CRO
• Knowledge of drugdevelopment process English knowledge
• Solid knowledge of clinical data management and
• Problem solving
• English Proficient
TYPE...
Regulatory Affairs on regulatory product landscape and strategies as a part of overall drugdevelopment strategy.
• Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts).
• Review...
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well:being of people...
Location: Ivrea, Italy
Role Purpose:
Leads and manages all Drug Product (DP) project activities linked to the development of radiopharmaceutical parenterals (both ready to use and freeze dried products). Supports & coaches team members, participates...
We are applying our TransCon technology to build a leading, fully integrated biopharmaceutical company focused on making a meaningful difference in patients’ lives. Guided by our core values of patients, science, and passion, we use our TransCon® drug...
to gain the best business value through technology-enabled solutions and achieve excellence in business operations.
Job Description
The role:
We are currently looking for a Senior Drug Safety Specialist to join our team. The ideal candidate will...
and cosmetics industries, with potential in other sectors.
A world leader in drug traceability, it supplies the leading global producers (over 50% of the top 20 multinationals) and various government authorities with solutions to monitor the supply chain...
regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of adverse events...
Our client, ONCOPEPTIDES AB (PUBL), is a biotech company focused on research, development, and commercialization of therapies for difficult-to-treat hematological diseases. The company uses its proprietary Peptide Drug Candidate platform...
an understanding of VAT requirements and differences across other EMEA countries.
• JDE experience.
• Spoken and written English to a professionally fluent level.
Inotiv is a growing contemporary drug discovery and development company where we “Play...
through to early life cycle submissions.
• Sound knowledge of drugdevelopment, manufacturing processes and quality control and may have a specialized area of expertise.
• Knowledge of worldwide CMC regulatory requirements and successful track record of...
Sponsor, in accordance with the Sponsor's Code of Conduct, Standard Operating Procedures (SOPs)/Working Practices (WPs), and local/country regulations; the SEM will contribute to the development and implementation of new SOPs/WPs as applicable
• Contribute...
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