EMPREGO ASSOCIATE I REGULATORY SUBMISSIONS

Provide expert regulatory input to strategic decision making, and ensure that regulatory strategies and regulatory activities are effectively executed to meet the...

Prepares and/or reviews regulatory documents to support clinical trial submissions... independently provides regulatory support for complex projects and programs...

⦁ acquire relevant exposure and / or expertise in pharmaceutical & medical device regulations & regulatory submissions management...   ⦁ demonstrated organizational...

Your responsibilities will include: represents ra on cross functional projects which may include product development, manufacturing process changes, site transfers...

Responsible for preparation and submission of regulatory applications, as well as internal regulatory file documentation...   prior experience with china and international...

Represents hovione through communications and negotiations with regulatory authorities, preparing, submitting and managing all matters related to regulatory submissions...

Come join a growing, global division and become a member of a large and experienced regulatory team! learn more about our urology division here: https://www...

Your responsibilities will include:  support sterilization process owner and global regulatory processes, responsibilities include the following: support regulatory...

Do you have experience in eu market regulatory affairs in the pharmaceutical sector? this offer is for you!we are currently recruiting for a client company in the...

Maintains awareness of regulatory guidelines and updates... experienced in eu market regulatory affairs (preferred)... support the site on the launch of new products...

The senior associate will collaborate with cross-functional teams, including sourcing, accounts payable, and finance, to ensure smooth and seamless financial operations...

In addition to the skills and experience above an associate principal should have... knowledge of regulatory guidance documents and scientific guidelines relating...

The benefit/risk associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of primevigilance...

As a sr associate software develoepr, you will... sr associate software developer - risk & quantitative solutions - hybrid ... as a valued member of this dynamic...

Good knowledge of clinical research regulatory requirements... evaluating the quality and integrity of site practices in accordance with regulatory requirements...

Your responsibilities will include: performing site selection, initiation, monitoring and close-out visits supporting the development of a subject recruitment plan...

In depth knowledge and skill in applying applicable clinical research regulatory requirements; i... manage the progress of assigned studies by tracking regulatory...

Review regulatory documentation and co-ordination of site documentation to support regulatory requirements... experience of working with regulatory affairs and a...

This includes maintaining, controlling and auditing training materials required for company and regulatory compliance... the business associate will be leading...