**Work mode**:**Onsite Location(s)**:Heredia, H, CR**Additional Locations**: N/A**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance**- At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer and has been recognized with the Catalyst Award in 2022, a prestigious recognition of diversity, equity and inclusion excellence. Also, we have a Gender Equality Policy to support our commitment.- Hybrid Roles:- Boston Scientific's hybrid workplace includes WFH and onsite. You will have the opportunity to discuss details in the interview.**About the role**:- This is an opportunity for those interested in gaining knowledge and experience about clinical data analysis and compliance with regulatory standards and guidelines for medical devices, and corporate standard operating procedures as they relate to clinical safety and risk management.- You will support, in a multicultural team environment, with the evaluation and analysis of clinical data for cardiology medical devices, helping in collaboration with other team members with updating clinical documentation that synthesizes information from multiple data sources. You will contribute, with guidance, on updating clinical evaluation plan (CEP) and report (CER) documents, and post-market clinical follow-up (PMCF) plan and reports, in alignment with applicable clinical and regulatory standards and business needs.-**You're Responsibilities include**:- Provides support to team members with updating clinical deliverables (PMCF Plan and Report, Clinical Evaluation Plan and Report) to comply with regulatory standards and corporate procedures, for different product families.- Help with literature review on products/product families to interpret and summarize harms, hazards, alternate therapies and device specific benefits from literature.- Serves as a liaison between team members and other cross-functional partners in support of obtaining additional input to aid in clinical risk analysis.**What We're Looking For**:- At least 60% of studies completed in biomedical engineering, clinical area (physician, pharmacist, nurse, etc.), scientific area.- English Level desired: B2+- Basic to intermediate knowledge/experience with Microsoft Office tools.- Available for a 6-month internship with the possibility of being extended to a maximum of one year- Available 38-40 hours per week**Requisition ID**:579902- **Benefits - Life-Work Integration - Community - Career Growth**- At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination, and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life's work.**Job Segment**:Data Analyst, Biomedical Engineering, Compliance, Medical Device, Law, Data, Engineering, Legal, Healthcare
