Offer summary

Qualifications:

Master's or PhD in a relevant clinical or scientific discipline., At least 6 years of experience in clinical research or R&D., Expertise in clinical study design, evidence generation, and regulatory compliance., Proficiency in biostatistics tools like STATA, SAS, or R..

Key responsibilities:

Lead clinical research activities to establish safety and efficacy criteria.

Design, initiate, and manage clinical studies aligning with regulatory and business goals.

Conduct literature reviews and appraise clinical evidence for product positioning.

Collaborate with cross-functional teams to integrate clinical strategies into product development.

Job description

We are seeking a Clinical Scientist to join our R&D Clinical Affairs team and contribute to the development of groundbreaking medical device technologies that transform patient care. The successful candidate will lead clinical development activities, working cross-functionally to generate high-quality clinical evidence that supports regulatory clearance, market adoption, and business growth.

Key Responsibilities:

Lead clinical research activities to establish safety and efficacy performance criteria for medical devices.
Design, initiate, and manage internal and external clinical studies, ensuring alignment with regulatory and business objectives.
Conduct systematic literature reviews and critical appraisals of clinical evidence to support product positioning and market expansion.
Collaborate with R&D, Regulatory Affairs, and Marketing to integrate clinical strategies into product development and commercialization plans.
Build and cultivate relationships with external experts, academic institutions, and research organizations.
Monitor competitive landscapes and provide insights into emerging trends and ongoing clinical studies.

What You’ll Bring:

Advanced degree (Master’s or PhD) in a relevant clinical or scientific discipline, with 6+ years of experience in clinical research or R&D.
Expertise in clinical study design, evidence generation, and regulatory compliance (e.g., FDA, ISO, GCP).
Strong knowledge of biostatistics and proficiency in tools like STATA, SAS, or R.
Excellent communication and collaboration skills, with the ability to work effectively in a matrixed environment.
Proven ability to think strategically, manage multiple projects, and deliver results in a dynamic setting.

So why join Hologic?

We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and annual bonus scheme, one of our talent partners can discuss this in more detail with you.

If you have the right skills and experience and want to join our team, apply today. We can’t wait to hear from you!

The annualized base salary range for this role is $110,900 - $175,100 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.

Agency and Third-Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

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