Vivify Talent

About Vivify Talent

Vivify is a recruitment firm in the pharmaceutical industry, working exclusively with talent and hiring teams in the complex data environment of drug development. Our specialism lies within Medical Writing and Biometrics where we are building talent communities to support one another through key changes and milestones in their careers.

9 Job openings in Vivify Talent

Regulatory Writer
Vivify Talent - Manama - Bahrain

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experience 0 - 0 years
Part Time
Salary Icon Not Disclosed

Lead the creation of top-tier regulatory documents, ensuring compliance with industry standards. Synthesize complex scientific data with precision in documents like clinical study reports, protocols, regulatory submissions, and marketing authorization applications. Collaborate sea More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply

Senior Medical Writer
Vivify Talent - Riyadh - Saudi Arabia

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experience 0 - 2 years
Part Time
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Lead the creation of top-tier regulatory documents, ensuring compliance with industry standards. Synthesize complex scientific data with precision in documents like clinical study reports, protocols, regulatory submissions, and marketing authorization applications. Collaborate sea More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply

Regulatory Writer
Vivify Talent - Kuwait City - Kuwait

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experience 0 - 0 years
Part Time
Salary Icon Not Disclosed

Lead the creation of top-tier regulatory documents, ensuring compliance with industry standards. Synthesize complex scientific data with precision in documents like clinical study reports, protocols, regulatory submissions, and marketing authorization applications. Collaborate sea More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply
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experience 0 - 0 years
Part Time
Salary Icon Not Disclosed

Regulatory Expertise: Leverage your in-depth knowledge of European regulations to contribute to the development of high-quality regulatory documents, including but not limited to clinical study reports, regulatory submissions, protocols, investigator brochures, and marketing authori More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply

Principal Regulatory Writer
Vivify Talent - Riyadh - Saudi Arabia

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experience 0 - 0 years
Part Time
Salary Icon Not Disclosed

As a Principal Regulatory Writer, you will play a pivotal role in translating complex scientific and clinical data into compelling regulatory documents. Your expertise will be crucial in ensuring compliance with European regulations and industry standards. Key Responsibilities: More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply
exclusion unfavorite
experience 0 - 0 years
Part Time
Salary Icon Not Disclosed

Lead the creation of top-tier regulatory documents, ensuring compliance with industry standards. Synthesize complex scientific data with precision in documents like clinical study reports, protocols, regulatory submissions, and marketing authorization applications. Collaborate sea More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply
exclusion unfavorite
experience 0 - 0 years
Part Time
Salary Icon Not Disclosed

Regulatory Expertise: Leverage your in-depth knowledge of European regulations to contribute to the development of high-quality regulatory documents, including but not limited to clinical study reports, regulatory submissions, protocols, investigator brochures, and marketing authori More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply

Senior Medical Writer
Vivify Talent - Kuwait City - Kuwait

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experience 0 - 0 years
Part Time
Salary Icon Not Disclosed

Lead the creation of top-tier regulatory documents, ensuring compliance with industry standards. Synthesize complex scientific data with precision in documents like clinical study reports, protocols, regulatory submissions, and marketing authorization applications. Collaborate sea More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply

Regulatory Writer
Vivify Talent - Riyadh - Saudi Arabia

exclusion unfavorite
experience 0 - 0 years
Part Time
Salary Icon Not Disclosed

Lead the creation of top-tier regulatory documents, ensuring compliance with industry standards. Synthesize complex scientific data with precision in documents like clinical study reports, protocols, regulatory submissions, and marketing authorization applications. Collaborate sea More...

Employer Active Posted on 28 Mar | Part Time | Easy Apply