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Director of Drug Development & Regulatory Strategy

labcorp

Full-time
USA
$180k-$230k per year
director
strategy
project management
leadership
documentation
Apply for this position

At Labcorp, we advance science, technology and innovation and are recognized as one of the most respected companies in the world.

We believe in the power of science to change lives. We are a leading global life sciences company that delivers answers to crucial health questions —because we know that knowledge has the potential to make life better for all. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

We have an excellent career opportunity for a Director of Drug Development & Regulatory Strategy to join our dynamic team!

This is a Remote US based position with approximately 20% travel.

This position is not eligible for visa sponsorship.

Position Summary

The Director of Drug Development and Regulatory Strategy is an individual contributor who will provide scientific and regulatory strategy leadership and direction to the client and to Labcorp Development Team(s) for potential and awarded programs. As an expert in drug development, they will provide clients with consultancy and advisory services to help them develop their compound(s) in an efficient and timely manner to achieve their goals, with an ability to guide the overall development strategy.

Being well versed in the regulatory requirements for nonclinical testing, they must have the ability to understand the scientific rationale for the development of a wide variety of compounds/modalities and understand the interplay between clinical and nonclinical plans. Expertise in nonclinical regulatory writing, supporting regulatory agency meetings & interactions and reviewing nonclinical regulatory documentation related to the US and EU processes is essential.

Minimum Education and Experience Requirements:

  • PhD in an appropriate scientific discipline and/or additional advanced degree.

  • 12-15 years scientific expertise demonstrated in the pharmaceutical industry, specifically related to the drug development process, with an emphasis on biopharmaceutical and ATMP, in addition to small molecule development.

    • Background and training in toxicology, immunology, vaccines, CMC, or DMPK.

  • 5+ years representing a functional area, such as Toxicology, CMC, Project Management, ADME, Regulatory Strategy on molecule development teams.

  • An up-to-date awareness of ICH and regional Regulatory Guidelines as well as industry trends is essential.

  • Demonstrated ability to get work done through influencing others.

  • Strong people skills (including teamwork, negotiation, communication, presentation)

  • Ability to work independently, often under pressure.

  • Proven leadership and personal initiative.

  • Project management training or certification is an advantage.

Application window open through: 10/22/2025

Pay Range: $180k - $230k annual salary (USD)

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. 

The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers.

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.  Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.  For more detailed information, please click here. 

Why People choose to work at Labcorp:  At Labcorp, it is our people that make us great – it is what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Apply for this position
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About the job

Full-time
USA
$180k-$230k per year
Posted 1 day ago
director
strategy
project management
leadership
documentation

Apply for this position

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Director of Drug Development & Regulatory Strategy

labcorp

At Labcorp, we advance science, technology and innovation and are recognized as one of the most respected companies in the world.

We believe in the power of science to change lives. We are a leading global life sciences company that delivers answers to crucial health questions —because we know that knowledge has the potential to make life better for all. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

We have an excellent career opportunity for a Director of Drug Development & Regulatory Strategy to join our dynamic team!

This is a Remote US based position with approximately 20% travel.

This position is not eligible for visa sponsorship.

Position Summary

The Director of Drug Development and Regulatory Strategy is an individual contributor who will provide scientific and regulatory strategy leadership and direction to the client and to Labcorp Development Team(s) for potential and awarded programs. As an expert in drug development, they will provide clients with consultancy and advisory services to help them develop their compound(s) in an efficient and timely manner to achieve their goals, with an ability to guide the overall development strategy.

Being well versed in the regulatory requirements for nonclinical testing, they must have the ability to understand the scientific rationale for the development of a wide variety of compounds/modalities and understand the interplay between clinical and nonclinical plans. Expertise in nonclinical regulatory writing, supporting regulatory agency meetings & interactions and reviewing nonclinical regulatory documentation related to the US and EU processes is essential.

Minimum Education and Experience Requirements:

  • PhD in an appropriate scientific discipline and/or additional advanced degree.

  • 12-15 years scientific expertise demonstrated in the pharmaceutical industry, specifically related to the drug development process, with an emphasis on biopharmaceutical and ATMP, in addition to small molecule development.

    • Background and training in toxicology, immunology, vaccines, CMC, or DMPK.

  • 5+ years representing a functional area, such as Toxicology, CMC, Project Management, ADME, Regulatory Strategy on molecule development teams.

  • An up-to-date awareness of ICH and regional Regulatory Guidelines as well as industry trends is essential.

  • Demonstrated ability to get work done through influencing others.

  • Strong people skills (including teamwork, negotiation, communication, presentation)

  • Ability to work independently, often under pressure.

  • Proven leadership and personal initiative.

  • Project management training or certification is an advantage.

Application window open through: 10/22/2025

Pay Range: $180k - $230k annual salary (USD)

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. 

The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers.

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.  Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.  For more detailed information, please click here. 

Why People choose to work at Labcorp:  At Labcorp, it is our people that make us great – it is what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

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