Job Title: Sr. Executive (Clinical) Medical Device Clinical Evaluation, Medical Writing and Publications. Location: Moraiya, Ahmedabad Job Type: Full-time Introduction: We are seeking a highly motivated and experienced PhD candidate with 3-4 years of experience to join our team, focusing on medical device clinical evaluation, medical/technical writing, publication writing and content creation. The ideal candidate will have a strong background in medical research, excellent writing skills, and a passion for communicating complex scientific information clearly and effectively. This is an exciting opportunity to contribute to cutting-edge developments in the medical device industry while supporting our clinical evaluation and content creation efforts. Key Responsibilities: Medical Device Clinical Evaluation:Contribute to the design, implementation, and reporting of clinical evaluation activities for medical devices for both planning and executionReview and analyze clinical data (State of Art Literature, Post market surveillance), ensuring compliance with regulatory requirements and industry standards.Collaborate with cross-functional teams, including R&D, regulatory affairs, and quality assurance and marketing/sales, to support clinical evaluation efforts.Assist in the preparation of Clinical Evaluation Reports (CERs) and accordingly publications/digital creations and promotional materials including all other regulatory documentation.Publication Writing:Draft, edit, and submit product related scientific publications for peer-reviewed journals, ensuring high-quality and accurate content.Collaborate with internal teams and external experts to develop manuscripts, posters, and presentations for medical conferences.Contribute to state of the art literature reviews and systematic reviews of point in question to support publication and research needs.To identify the journals for the publication of draft manuscripts.Medical Writing:Produce high-quality medical writing for various purposes, including regulatory submissions, clinical trial protocols, and other technical documents.Ensure all medical writing complies with relevant guidelines and standards, including Good Clinical Practice (GCP) and ISO/ICH standards.Develop clear and concise clinical and scientific documentation for both technical and non-technical audiences.Medical Content, Promotional & Blog Writing:Review the state-of-the-art literature, align it with post-market reviews of the products, collaborate with the risk management team, and ensure the review and documentation of the product IFU meet the state-of-the-art claim/indications requirements.Create engaging, informative, and scientifically accurate blog posts and articles related to medical devices, healthcare innovations, clinical evaluations, and related topics.Work with the in house teams to produce content that educates and informs our audience, enhances brand awareness, and supports thought leadership in the medical device sector.Literature Writing:Conduct literature reviews, summarize key findings, and identify emerging trends in medical device technology, clinical practices, and regulatory frameworks.Contribute to the preparation of white papers, technical reports, and other literature-based documents.PhD in a relevant field (e.g., Medical Sciences, Life Sciences, Biomedical Engineering, Pharmacology, etc.).3-4 years of experience in medical device clinical evaluation, medical writing, or related fields.Strong understanding of regulatory guidelines, clinical evaluation methodologies, and the medical device industry.Proven track record of publishing in scientific journals and presenting at conferences.Exceptional writing and editing skills, with attention to detail and ability to simplify complex scientific concepts.Experience with literature review and systematic review methodologies.Ability to work independently and as part of a multidisciplinary team.Familiarity with medical content creation, including blogs, articles, and other digital content.Proficiency in Microsoft Office Suite and relevant writing software (e.g., EndNote, Reference Manager).Preferred Skills: Experience with clinical evaluation reports (CERs) and regulatory submissions (e.g., FDA, EMA).Familiarity with medical device regulations, standards, and industry guidelines (ISO 13485, MDR, etc.).Experience with content management systems (CMS) and SEO best practices.Strong organizational skills with the ability to manage multiple projects simultaneously and meet deadlines.Why Join Us: Opportunity to work at the forefront of medical device innovation and clinical evaluation.Collaborative and dynamic work environment with the potential for professional growth and development.Contribute to impactful publications and content that drive industry advancements.Competitive compensation and benefits package.How to Apply: Interested candidates are invited to submit a CV, cover letter, and writing samples (e.g., published articles, clinical reports, or other relevant work) to gm@aegis-lifesciences.com. We look forward to reviewing your application!

Key roles and responsibilities:1. Intellectual Property Rights ManagementConduct thorough research to identify potential intellectual property rights (IPR) issues and opportunities.Assist in the development, implementation, and enforcement of IPR strategies for the companys products and services.Work with internal teams and external consultants to ensure proper protection of intellectual property assets.Provide advice and guidance on issues related to intellectual property rights.Draft, file, and prosecute Patent Cooperation Treaty (PCT) applications to secure international patent protection for clients across multiple jurisdictions.Assist in preparing detailed technical descriptions and claims for patent filings, ensuring compliance with global patent standards.Coordinate with international law firms and patent offices to manage the filing and prosecution of international patent applications under the PCT.Monitor deadlines for PCT national phase entry and ensure timely responses to office actions or objections raised by foreign patent offices.Advise clients on strategic options related to international patent protection, including the selection of countries for patent filing based on business goals. 2. Trademark and Patent WritingIdentify, draft and prepare patent and trademark applications, ensuring compliance with all applicable laws and regulations.Work closely with inventors to understand and document innovations for patent applications.Conduct patent and trademark searches to ensure the novelty of inventions and designs.Review and analyze existing patents, trademarks, and copyrights to ensure proper protection of intellectual property assets.Assist in the preparation of responses to patent office actions via external consultant, office communications, and related documentation.Manage the filing of trademark applications across various jurisdictions worldwide, ensuring that all filings comply with the respective countrys requirements.Research and identify appropriate classes and descriptions for international trademarks to maximize protection and minimize legal challenges.Coordinate with local counsel and international trademark authorities for the preparation and filing of Madrid Protocol or National trademark applications.Track and manage the progression of international trademark applications, respond to office actions, and monitor oppositions and cancellations.Advise clients on best practices for protecting their trademarks internationally, taking into account the scope of rights, market presence, and risks of infringement.Conduct comprehensive trademark searches globally to identify potential conflicts and advise clients on the likelihood of successful registration.Develop international trademark strategies tailored to clients global business objectives, ensuring robust protection against infringement and counterfeiting.3. IPR Documentation and FilingEnsure timely filing of intellectual property applications with the relevant authorities.Maintain an up-to-date record of all filed applications, patents, trademarks, and related correspondence.Manage and track deadlines for renewals and legal actions related to intellectual property protection.4. Copywriting and Content CreationWrite clear and concise copy for marketing, legal, and informational purposes, while adhering to company brand guidelines.Develop creative and persuasive copy for patent descriptions, trademark filings, and other legal documents.Ensure all copywriting materials are legally sound, fact-checked, and aligned with intellectual property guidelines.5. Legal Research and AnalysisStay updated on the latest trends, laws, and regulations in intellectual property, patents, and trademarks.Perform legal research to support trademark and patent applications, including international filings.Assist in the preparation of reports and summaries regarding IPR issues and opportunities.6. Collaboration and CommunicationCollaborate with internal stakeholders (e.g., R&D, regulatory/Quality) to provide IPR-related guidance.Communicate with external legal counsel and government bodies to support the registration and defense of patents, trademarks, and copyrights.Provide ongoing support for IP litigation and dispute resolution, as needed.Key Requirements:Proven experience in intellectual property rights, particularly in trademark and patent writing and searches.Strong understanding of IPR laws and regulations, including local and international guidelines.Excellent written and verbal communication skills, with a knack for copywriting and drafting legal documents.Strong attention to detail and the ability to manage multiple projects simultaneously.Ability to work independently and as part of a collaborative team.Proficient in IP management software and Microsoft Office Suite.Knowledge of the patent application process and familiarity with patent databases (e.g., USPTO, WIPO) is a plus.Ability to work in a fast-paced, demanding, timeline-driven environmentInnovative and creative mindsetAn ability to work effectively with an internal and external of stakeholdersPossesses excellent science communication, organization, management, and administrative skills.Excellent interpersonal, communication, writing, and presentation skillsAbility to work and perform within a disciplinary and cross disciplinary teamAbility to prioritize work, meet deadlines and produce quality results on time with attention to detail.