VOICES

Explore our FDA-focused solution areas to see how we support medical device and pharmaceutical companies across regulatory pathways and product types, from early strategy through approval-ready submissions.

VOICES

Explore our FDA-focused solution areas to see how we support medical device and pharmaceutical companies across regulatory pathways and product types, from early strategy through approval-ready submissions.

Join our Team

Marketing Manager

Marketing Manager

Lead complex regulatory submissions that set new standards for excellence.

Location

Philadelphia and Remote

Your Mission

Own and execute BSC’s marketing efforts across content, website, case studies, and thought leadership. Translate complex statistical and regulatory expertise into clear, credible messaging that positions BSC as a trusted leader in regulatory biostatistics.

About the Role

You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes. This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

You’ll contribute to study design, statistical analysis plans, regulatory submissions, and FDA interactions across medical device and life-science programs. Projects range from early feasibility through pivotal trials and post-submission support, often involving non-standard designs, external controls, or complex evidentiary challenges.

  • You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes.

  • This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

What You’ll Work On

You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes. This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

You’ll contribute to study design, statistical analysis plans, regulatory submissions, and FDA interactions across medical device and life-science programs. Projects range from early feasibility through pivotal trials and post-submission support, often involving non-standard designs, external controls, or complex evidentiary challenges.

  • You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes.

  • This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

How We Work

You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes. This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

You’ll contribute to study design, statistical analysis plans, regulatory submissions, and FDA interactions across medical device and life-science programs. Projects range from early feasibility through pivotal trials and post-submission support, often involving non-standard designs, external controls, or complex evidentiary challenges.

  • You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes.

  • This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

What We Look For

You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes. This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

You’ll contribute to study design, statistical analysis plans, regulatory submissions, and FDA interactions across medical device and life-science programs. Projects range from early feasibility through pivotal trials and post-submission support, often involving non-standard designs, external controls, or complex evidentiary challenges.

  • You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes.

  • This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

Why BSC®

You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes. This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

You’ll contribute to study design, statistical analysis plans, regulatory submissions, and FDA interactions across medical device and life-science programs. Projects range from early feasibility through pivotal trials and post-submission support, often involving non-standard designs, external controls, or complex evidentiary challenges.

  • You’ll work on high-impact clinical and regulatory programs where statistical decisions directly influence FDA outcomes.

  • This role sits at the intersection of biostatistics, clinical development, and regulatory strategy, with responsibility for shaping analyses that must withstand real regulatory scrutiny.

Testimonials

See what our sponsors say about BSC

On Experience

Battle ground tested. There is nothing that David and team haven't seen over the years – good bad and ugly.

• VP, Clinical Operations

• CEO, Medical Device Company

• Former FDA Regulator

Questions answered

Any other question?

Let's help you find a path

to market

  • About BSC®

    Working With BSC®

    Services

    Project logistics

    Data and Software

  • What does BSC specialize in?

    What types of clients do you work with?

    What therapeutic areas do you cover?

    How is BSC different from a CRO?

    What size projects do you handle?

Questions answered

Any other question?

Let's help you find a path

to market

  • About BSC®

    Working With BSC®

    Services

    Project logistics

    Data and Software

  • What does BSC specialize in?

    What types of clients do you work with?

    What therapeutic areas do you cover?

    How is BSC different from a CRO?

    What size projects do you handle?

Questions answered

Any other question?

Let's help you find a path

to market

  • About BSC®

    Working With BSC®

    Services

    Project logistics

    Data and Software

  • What does BSC specialize in?

    What types of clients do you work with?

    What therapeutic areas do you cover?

    How is BSC different from a CRO?

    What size projects do you handle?

Questions answered

Any other question?

Let's help you find a path

to market

  • About BSC®

    Working With BSC®

    Services

    Project logistics

    Data and Software

  • What does BSC specialize in?

    What types of clients do you work with?

    What therapeutic areas do you cover?

    How is BSC different from a CRO?

    What size projects do you handle?

Biomedical Statistical Consulting®
Biomedical Statistical Consulting®
Biomedical Statistical Consulting®
Biomedical Statistical Consulting®

Security

Robust data security and confidentiality

across sensitive, FDA-regulated clinical and regulatory data.

Disciplined security practices aligned with industry standards to protect confidential patient, sponsor, and regulatory information.

Disciplined security practices aligned with industry standards to protect confidential patient, sponsor, and regulatory information.

GDPR

SOC2 - in progress

For more information visit our trust center

Security

Robust data security and confidentiality

across sensitive, FDA-regulated clinical and regulatory data.

Disciplined security practices aligned with industry standards to protect confidential patient, sponsor, and regulatory information.

Disciplined security practices aligned with industry standards to protect confidential patient, sponsor, and regulatory information.

GDPR

SOC2 - in progress

For more information visit our trust center

Security

Robust data security and confidentiality

across sensitive, FDA-regulated clinical and regulatory data.

Disciplined security practices aligned with industry standards to protect confidential patient, sponsor, and regulatory information.

Disciplined security practices aligned with industry standards to protect confidential patient, sponsor, and regulatory information.

GDPR

SOC2 - in progress

For more information visit our trust center

Security

Robust data security and confidentiality

across sensitive, FDA-regulated clinical and regulatory data.

Disciplined security practices aligned with industry standards to protect confidential patient, sponsor, and regulatory information.

Disciplined security practices aligned with industry standards to protect confidential patient, sponsor, and regulatory information.

GDPR

SOC2 - in progress

For more information visit our trust center

Request Expert Review

Backed by Regulatory Experience.

Engage directly with senior biostatisticians to review your clinical strategy, statistical approach, or FDA submission — with clarity, rigor, and regulatory perspective.

Confidential discussion with senior biostatisticians experienced in FDA submissions.

Request Expert Review

Backed by Regulatory Experience.

Engage directly with senior biostatisticians to review your clinical strategy, statistical approach, or FDA submission — with clarity, rigor, and regulatory perspective.

Confidential discussion with senior biostatisticians experienced in FDA submissions.

Request Expert Review

Backed by Regulatory Experience.

Engage directly with senior biostatisticians to review your clinical strategy, statistical approach, or FDA submission — with clarity, rigor, and regulatory perspective.

Confidential discussion with senior biostatisticians experienced in FDA submissions.

Request Expert Review

Backed by Regulatory Experience.

Engage directly with senior biostatisticians to review your clinical strategy, statistical approach, or FDA submission — with clarity, rigor, and regulatory perspective.

Confidential discussion with senior biostatisticians experienced in FDA submissions.