Clinical Development Scientist
1 week ago
Clinical Development Scientist (San Diego, CA)
The Clinical Development Scientist will be responsible for supporting evidence-generation processes for New Product Introduction (NPI) and Life Cycle Management (LCM) initiatives, working under direct supervision of the Clinical Development Manager, Clinical Affairs. The role performs literature searches, analyzes clinical data, and contributes to the development of robust clinical plans aligned with project objectives. The role collaborates actively with cross-functional teams, handles clinical studies, and assists in authoring Clinical Evaluation Reports (CERs) and regulatory submissions. The role troubleshoots data-related issues, understands global clinical evidence requirements, and presents findings to stakeholders.
Your role:
- Perform comprehensive literature searches and in-depth reviews to support evidence-generation processes for both New Product Introduction (NPI) and Life Cycle Management (LCM) initiatives, working under direct supervision.
- Analyze clinical data meticulously and contribute substantively to the development of robust clinical plans that align with project objectives.
- Collaborate actively with cross-functional teams to develop comprehensive NPI clinical deliverables, including meticulously crafted validation plans and clinically sound evaluation plans.
- Monitor and perform day-to-day management of assigned clinical studies, ensuring seamless coordination with Clinical Operations (Clin Ops) and Biostatistics & Data Management (BS&DM) teams.
- Document meticulously and provides valuable assistance in crafting Clinical Evaluation Reports (CERs), Clinical Study Reports (CSRs), and clinical sections of regulatory submissions.
- Troubleshoot issues related to clinical data collection, analysis, and reporting, ensuring the integrity and accuracy of study outcomes.
- Develop a profound understanding of global clinical evidence requirements and regulatory pathways to inform strategic decision-making and compliance efforts.
- Presents findings eloquently and provides cogent recommendations from literature reviews and data analyses to internal stakeholders, fostering informed decision-making processes.
- Acquire and apply extensive domain knowledge in technology and/or therapeutic areas, leveraging it effectively to support and enhance clinical development activities.
- Interact closely with colleagues to determine and implement optimal approaches for evidence generation and clinical study design, fostering a culture of innovation and excellence.
You are the Right Fit:
- Bachelor's Degree in Life Sciences or Healthcare Related Fields with at least 4 years of experience in the medical device industry. MS Degree with at least 2 years of related experience.
- Awareness of importance of IP generation and protection / in identifying and initiating new methods of diagnosis, treatment and/or care
- Experience with clinical data analysis.
- Understanding of the needs and operations related to a clinical study.
- Familiarity with the following therapeutic areas: Pacemakers, Defibrillators, Cardiac Resynchronization Therapy, Electrophysiology, Holter Monitoring, Ambulatory ECG preferred.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
- Learn more about our business.
- Discover our rich and exciting history.
- Learn more about our purpose.
- Read more about our employee benefits.
If you're interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.
Philips Transparency Details
The pay range for this position is $78,000 to $120,000, annually. The actual base pay offered may vary depending on multiple factors including, job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here.
At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.
Additional Information
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to San Diego, CA.
This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.
Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.
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