Clinical Scientist

US-NJ-Princeton-100-Headquarters

Full time

JR-6666

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

SUMMARY DESCRIPTION

The Clinical Scientist supports the planning and execution of clinical evidence programs for products across the Tissue Reconstruction portfolio. This role contributes to study design, protocol development, study execution, data analysis, and interpretation of clinical and real-world data to support regulatory, medical, commercial, and market access objectives.

The scientist works closely with Clinical Development leadership within Medical Affairs and collaborates cross-functionally with downstream Medical Affairs colleagues, as well as Regulatory Affairs, Clinical Operations, Biostatistics, R&D, Marketing, Market Access, and external clinical partners to generate evidence supporting product development, regulatory submissions, clinical claims, scientific communications, reimbursement initiatives, and evidence-based decision-making across the product lifecycle. In addition to traditional clinical studies, the role may contribute to real-world evidence, registry, health economics, outcomes research, and claims-based research initiatives.

The scientist leverages strong analytical and scientific skills to derive insights from diverse data sources and support evidence generation, investigator collaborations, and scientific publications that advance patient care and product adoption.

SUPERVISION RECEIVED

Reports to Medical Strategy Lead

SUPERVISION EXERCISED

None

KEY RESPONSIBILITIES

• Contribute to the development and execution of clinical evidence strategies supporting products across the Tissue Reconstruction portfolio.

• Conduct literature reviews, evidence gap assessments, and scientific landscape analyses to inform evidence-generation priorities.

• Lead the scientific design of assigned studies and contribute to the development of protocols, data collection instruments, analysis plans, and study reports in collaboration with Clinical Operations, Medical Communications, and Biostatistics.

• Design, plan, and execute clinical studies, registries, real-world evidence, outcomes research, and claims-based research initiatives.

• Lead assigned study and evidence-generation workstreams with accountability for timelines, deliverables, study quality, and execution.

• Analyze, interpret, and synthesize clinical, real-world, health economics, and published data to generate scientific insights regarding evidence gaps, competitive evidence evaluations, and landscape analyses to inform clinical development and evidence strategy.

• Contribute to scientific publications, conference presentations, and other evidence dissemination activities.

• Present scientific findings and evidence-based recommendations to internal stakeholders and cross-functional teams.

• Collaborate with Medical Affairs, Regulatory Affairs, Clinical Operations, Biostatistics, R&D, Marketing, Market Access, and external investigators to align evidence-generation activities with product development and business needs.

• Support investigator and KOL collaborations through study planning discussions, advisory activities, and investigator-initiated research programs.

DESIRED MINIMUM QUALIFICATIONS

• Advanced degree required (Master's minimum; Ph.D. preferred) in Biomedical Engineering, Biomaterials, Tissue Engineering, Regenerative Medicine, Biological Sciences, Public Health, Epidemiology, Health Outcomes Research, or a related scientific discipline.

• Minimum of 3 years of relevant experience in clinical development, clinical research, medical affairs, epidemiology, health outcomes, real-world evidence, or related evidence-generation functions.

• Experience supporting clinical studies, registries, real-world evidence (RWE), outcomes research, health economics, or claims-based research projects preferred..

• Experience within the medical device or biotechnology industry preferred.

• Demonstrated academic training, research experience, or scientific expertise in biomaterials, tissue engineering, regenerative medicine, wound healing, tissue repair, soft-tissue reconstruction, or related fields strongly preferred.

• Experience developing scientific communications, including manuscripts, abstracts, posters, presentations, reports, or literature reviews preferred.

TECHNICAL COMPETENCIES

• Strong analytical, critical-thinking, and scientific problem-solving skills.

• Knowledge of clinical research methodology, study design, and evidence-generation principles.

• Understanding of biostatistics and experience interpreting clinical, real-world, and published data.

• Ability to apply scientific understanding of biomaterials, tissue remodeling, and regenerative mechanisms to clinical evidence generation, study design, data interpretation, and scientific communications.

• Ability to synthesize complex clinical and scientific information into clear, actionable insights and recommendations.

• Ability to conduct literature reviews, evidence gap assessments, scientific landscape analyses, and evidence synthesis activities.

• Proactive, self-motivated, and results-oriented with a strong commitment to execution excellence.

• Familiarity with real-world evidence, outcomes research, registry, claims-based, and health economics research methodologies.

• Effective project management and organizational skills, with the ability to manage multiple priorities and deadlines.

• Strong scientific writing skills with the ability to support publications, abstracts, study reports, and scientific presentations.

• Excellent collaboration skills and demonstrated success working in a cross-functional, matrixed environment.

• Ability to build productive relationships with internal stakeholders, external investigators, and research partners.

• Excellent written, verbal, and presentation communication skills.

• Experience working with clinical, real-world, registry, or claims data and utilizing analytical or data visualization tools (e.g., Excel, R, SAS, SQL, Power BI, Tableau, or similar).

PHYSICAL REQUIREMENTS

The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills required of this position to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.

Must be able and willing to travel up to 20% of work time. Travel may occasionally occur outside of normal business hours, including weekends. While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, and walk through airports etc.

ADVERSE WORKING CONDITIONS

The adverse working conditions listed in this section include, but are not limited to, those environmental conditions to which the employee may be exposed while undertaking the essential duties and responsibilities of this position, which is that of a general plant environment. Adverse exposure may result from the handling of hazardous and biohazardous materials that include, but are not limited to, flammable and corrosive liquids, compressed gases, sharps, and medical wastes.

Work environment involves exposure to potentially dangerous materials that require following important safety precautions. Frequently required to use personal protective equipment to prevent exposure to biohazardous materials.

SELECTION GUIDELINES

Formal application, rating of education and experience; oral interview and reference check; job related tests may be required.

DISCLAIMER

The duties listed above are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.

The job description does not constitute an employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change.

Salary Pay Range:

$82,000.00 - $113,000.00 USD Salary

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training . In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation . Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences (

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

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Unsolicited Agency Submission

Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate’s name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

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Whatever your specialty, you’ll find an ideal setting for building a rewarding career.

Along the way, you’ll have the satisfaction of knowing your work matters, that it’s making patients’ lives better, making a positive and lasting difference. You’ll find that the pace is exhilarating – because the need is so urgent. You’ll be challenged – and supported – by the most dynamic and inspiring people in your profession. And you’ll grow a career that is more impactful and fulfilling then you thought possible. More than 4,200 Integra employees already know we’re a great place to build a career. Here’s your chance to discover that for yourself.