About the CompanyStrand Life Sciences is a genomics-based research and diagnostics company with a mission to improve global health by decoding the genetic information contained in an individualas genome. We have partnered with thousands of academicians and physicians to apply next-generation genomics to generate valuable insights into disease areas such as cancer, cardiovascular and metabolic diseases, eye and neurological disorders. Our partnership programs enable large-scale genomics research studies About the Position Strand is seeking to add Business Development Officer / Business Development Manager for Bangalore and Kerala. The roles will report into the Regional Sales Manager. He/she will be responsible for defining and executing the go-to-market plan for the region in order to achieve the assigned sales targets. They will be responsible for establishing MOUs and other strategic deals with healthcare institutions & KOLs. They will operate ethically and be motivated by and give the highest priority to the overall well-being of the patients. Job Requirements1. Achieve monthly, quarterly, and yearly targets in the assigned geographical regionDetermine the market potential for the region, prioritize the portfolio opportunities, and develop and execute the go-to-market plan.2. Drive optimal operating mechanisms to monitor and track progress of opportunities in the pipeline; and deliver on fulfilment targets.3. Develop and grow trusted relationship with senior Clinicians and other Key Opinion Leaders (KOL) in core areas4. Establish MOUs and grow business engagement with key healthcare customers by understanding customer challenges and delivering solutions. 5. Nurture relationship with professional society stakeholders within geographical area.6. Plan and conduct regional and local marketing events, including roundtables and client-site functions, in collaboration with Marketing team 7. Stay abreast of the latest in Next Generation Sequencing and standard of care in Prenatal and pediatric genetics.8. Be completely accountable for each sample/case ensuring it progresses within prescribed timelines from order to reporting9. Act as a primary customer point of contact in the region and ultimately be accountable for issue resolution for assigned region.Required Skills1. 0 to 3+ years of experience in the Molecular Diagnostics Industry2. Experience in and knowledge of Reproductive and Rare Disease is preferred, but not mandatory3. Good understanding of the genetic testing landscape4. An academic degree in Science in general, and biotechnology in particular, would be a plus5. Willingness to travel 70% of work time6. Good written and verbal communication skills in English language; fluency in local language is preferable What Strand Life Sciences offers1. Exciting opportunities for development and professional growth within our dynamic organization,2. Vibrant multidisciplinary scientific interaction and learning opportunity3. A collaborative and solution-oriented environment where you can make a difference,4. A lot of our studies are translational research studies involving cutting edge research problems in genomics of clinical conditions and drugs, with the opportunity to innovate constantly on the job as opposed to repeated monotonous execution of set processes,5. An innovative and open culture in a truly multicultural environment,6. A competitive salary and generous benefits

Job ResponsibilitiesThe Clinical Research Associate/Scientist will be responsible for: ScopingHelp the team in rapid and accurate feasibility analysis ofupcoming projects. Example projects are in the areas ofOncology, Reproductive health, metabolic disorders,neurodegenerative diseases etc often involving somegenomics component to the study design,This involves engaging with investigators across the country,and getting reasonably accurate estimates of recruitment rates,often for difficult indications.2. Planning and SetupContribute in planning and setting up of new clinical studiesincluding drafting/refining the study related documents and ECdossiers,Identify candidate sites and engage with PIs and site CRCs toassess feasibility for shortlisting sites, negotiate with sites todraft agreements for engagement,Put together necessary documentation for EC submissions andassist site teams as needed to ensure EC approvals areobtained in a timely mannerRegular and prompt performing quality control (QC) checks onclinical data received. This involves reviewing the data foraccuracy, consistency, and completeness, ensuring that allentries are correctly documented and any discrepancies orerrors are identified and addressed in a timely manner.Collaborate with other team members to resolve any issuesand ensure compliance with regulatory requirements.Plan the setup of other systems and processes for the smoothrunning of the trial including where needed setup of systemssuch as IVRS/IWRS, EDC for electronic CRFs, drafting ofstudy documents, ISF etc. and take care of site initiationactivities.Put together the necessary documentation for regulatorycompliance submissions like DCGI/CTRI/HMSC etc.,Manage vendors, contracts and sourcing and help in budgetingand meticulous planning of projects to ensure smoothimplementation and execution of the studies.3. Implementation & ExecutionImplement processes for efficient conduct of clinicalprojects/trials,Take care of necessary activities for training of site staffs andconducting the Site Initiation,Ensure that for each study, each site, each subject the datacollection, data validation and monitoring is diligently done,Troubleshoot issues faced in clinical studies in a timely mannerlike recruitment of subjects using innovative ideas like puttingin place systems to rigorously screen patients in OPDs, settingup referral networks with hospitals having substantial patientload, and working with investigators with different ideas forrecruitment,Ensure adherence to GCP guidelines to carry out high qualityclinical studies following good ethical practices,Ensure smooth handling and reporting of SAEs, payments ofmedical expenses, compensation, etc keeping record of thesame for audit purpose,Track and update status of the studies, identify challenges,record issues with issue resolution matrix and discuss potentialsolutions in internal meetings, customer meetings etc.,Manage the costs and timelines of implementation in line withthe original proposal for the projectEnsure that SOPs for the clinical studies are up-to-date andwork with relevant team members for conducting the study inaccordance with the SOPEnsure proper training of new team members, take care ofdocumentation and records for sponsor audits, regulatoryinspections and ensure that all the study records arediligently maintained for posterityCandidates Requirements Ph.D. degree in life sciences, fresher or with an experience of 1-2years in oncology or clinical trials management Ability to successfully manage/work simultaneous trials and meetdeadlines Clinical Data Management experience preferably as part of a CROteam in more than one therapeutic area would be an advantage Excellent understanding of clinical trials methodology, GCP (GoodClinical Practice), GDMP (Good clinical data management practice)and medical terminology Have comprehensive knowledge of clinical guidelines like NDCT(New Drugs and Clinical Trials) rules, ICMR guidelines, DCA (Drugsand Cosmetics Act) and procedures involved with relevant Govtregulatory bodies is desirable and will be an added advantage Good organizational skills as the job profile involves lot ofdocumentation and recording of information through computerizedprocesses of clinical trial management systems and electronic datacapture High attention to details and a strong analytical mind set Demonstrates comprehensive knowledge of capturing and storingclinical information Excellent proficiency in English language Demonstrated experience of working in multicultural andmultidisciplinary environments Dynamic team player with excellent communication and networkingskills, flexible mindset and scientifically curious Willing to travel within city and outside as required (job demands 50%or travel and may require extended period of stay at a site locationbased on project need)

About Strand Life Sciences:Strand is a 24-year-old spin-off from the Indian Institute of Science. We are a cutting-edge Genomics company with a global customer base. We build applications that use DNA sequencing to improve human health. In the process, we build algorithms, data pipelines, and visualizations to handle large amounts of sequence data. We are committed to transforming complex data into actionable insights, contributing to groundbreaking research and innovative solutions in the field of genomics. We anticipate that in the next few years, hundreds of millions of individuals will have their DNA sequenced, and invite you to join us in this transformative journey.About the PositionWe are looking for a talented and creative Content Creator/Writer to develop compelling, engaging, and high-quality content across various digital platforms. The ideal candidate should have a strong command of language, a knack for storytelling, and the ability to create content that resonates with the target audience.Key Responsibilities: Research and develop long-form and short-form digital content such as case studies, whitepapers, brochures, blogs, LinkedIn posts, etc Perform literature reviews on various bioinformatics and genomics technologies and developinformative blogs/social media posts. Regularly interact with internal project teams to stay up to date on products and services Proven ability to translate complex scientific concepts into engaging content for differentaudiences Resourceful, organized, and motivated to enhance sales opportunities, and look for new andcreative ways to expand our client portfolio. Collaborate with technical, design, and sales teams to align content with brand guidelines and strategy. Repurpose long-form content into bite-sized posts, infographics, and videos for multiplechannels. Conduct interviews, write case studies, and develop thought leadership articles. Conduct research on industry trends and competitor analysis to inform and optimize contentdevelopment efforts. Stay updated with the latest content marketing trends and digital storytelling techniques.Requirements: Masters (2-3 Years Exp.) or PhD (0-2 Years Exp.) in Life Sciences, Biotechnology, or a related field from a reputed institute Proven experience in content writing, copywriting, or content marketing in genetics. Excellent writing, editing, and proofreading skills with a strong attention to detail. Ability to write for different audiences and adapt tone and style accordingly. Familiarity with content management systems (CMS) such as WordPress. Basic knowledge of design tools like Canva or Adobe Suite is a plus. Strong time management skills with the ability to meet deadlines.Preferred Skills: Experience in writing for specific industries (e.g., biotech, pharma, diagnostics). Knowledge of social media marketing and content distribution strategies. Ability to create video scripts and multimedia content. Understanding of SEO best practices and content optimization techniques.We offer An innovative and open culture in a truly multicultural environment An opportunity to make a fundamental impact on human health Vibrant multidisciplinary scientific interaction and learning opportunity A collaborative and solution-oriented environment where you can make a difference A competitive salary and generous benefits

About Strand Life Sciences:Strand is a 24-year-old spin-off from the Indian Institute of Science. We are a cutting-edge Genomics company with a global customer base. We build applications that use DNA sequencing to improve human health. In the process, we build algorithms, data pipelines, and visualizations to handle large amounts of sequence data. We are committed to transforming complex data into actionable insights, contributing to groundbreaking research and innovative solutions in the field of genomics. We anticipate that in the next few years, hundreds of millions of individuals will have their DNA sequenced, and invite you to join us in this transformative journey.Strand has built bioinformatics software for most analytics platforms: microarrays, mass spectrometry, next-generation sequencing, high throughput microscopy, and digital PCR, covering the spectrum from genomics, transcriptomics, epigenomics, and systems biology.With our position as a leading provider of diagnostics services, biomarkers, and bioinformatics, we intend to improve the healthy life spans of a million individuals in the coming decade.About the PositionStrand is looking for a Project Manager to join our team. The qualified candidate will facilitate content management and operations and thus drive content marketing initiatives in different avenues - conference engagement, website, and social media.The critical goals of the US commercial team at Strand are identifying new leads, pitching products and services, engaging with new clients, and maintaining relationships with existing customers.The role will report to the Content Lead of the Business Development US commercial team headed by the VP of Business Development. Key Responsibilities:Ensure the execution of deliverables, based on the content calendar, from the content team and internal project teams.Responsible for end-to-end execution of content and logistics associated with conferences - abstract submissions, poster presentations, slide decks, and physical content.Consult with Sales and Project teams to organize promotional activities such as conference booth events, webinars, talks, etc. Responsible for briefing the team leads and/or Project POCs about required deliverables and consistently following up.Develop timelines and coordinate material transfer between Strand teams and the Design firm while strictly adhering to internal and external deadlines. Drive weekly tracking of deliverables from Design.Key Skills & Qualifications:Graduate / Postgraduate degree in Management/Life Sciences/Bioinformatics2-3 years of post-graduate experience in project management and operationsProven ability to manage complex projects while leveraging effective communication skills a high attention to detail Excellent interpersonal and stakeholder management skills.Preferred Experience:Additional qualifications such as PMP certification and/or an MBA Experience working in medical writing/scientific communicationsExperience with working with cross-cultural teams and navigating multiple time zones (PST/IST)We offerAn innovative and open culture in a truly multicultural environmentAn opportunity to make a fundamental impact on human healthVibrant multidisciplinary scientific interaction and learning opportunityA collaborative and solution-oriented environment where you can make a differenceA competitive salary and generous benefits

About Strand Life Sciences:Strand is a 24-year-old spin-off from the Indian Institute of Science. We are a cutting-edge Genomics company with a global customer base. We build applications that use DNA sequencing to improve human health. In the process, we build algorithms, data pipelines, and visualizations to handle large amounts of sequence data. We are committed to transforming complex data into actionable insights, contributing to groundbreaking research and innovative solutions in the field of genomics. We anticipate that in the next few years, hundreds of millions of individuals will have their DNA sequenced, and invite you to join us in this transformative journey.About the PositionWe are seeking a motivated and detail-oriented Associate Application Scientist Support to join our growing team. The ideal candidate will provide technical and scientific support, ensuring they maximize the value of our products and solutions. As an entry-level role, you will work closely with senior scientists & support teams to troubleshoot technical issues, provide product demonstrations, and assist with application development. This is an excellent opportunity to build a career in scientific support and application science.Key Responsibilities: Customer Support: Provide first-line technical support via email, phone, or video calls.Troubleshoot and resolve issues related to the application of our products, working withother teams as needed for complex issues. Technical Assistance: Assist with product installations, configurations, and maintenance.Guide them through the best practices for using the product in their specific applications. Product Demonstrations: Assist with product demonstrations, including in-person andvirtual sessions, showcasing key product features and how they benefit customers. Application Development: Assist in evaluating and optimizing workflows and applicationsto improve product performance. Collaborate with internal teams to identify and resolveproduct limitations or enhancement opportunities. Feedback Collection: Gather and document customer feedback to contribute to productimprovements and new feature requests. Collaborate with the product development teamto relay customer needs and issues. Collaboration: Work closely with the R&D, Sales, and Marketing teams to ensure a cohesiveapproach to customer support and communication.Qualifications & Skills Required Understanding on Bioinformatics & Zeal for software technical support Education: Bachelors degree in a relevant scientific field (e.g., Biology, Chemistry,Biochemistry, Life Sciences, or similar). Experience: 0-2 years of experience in a scientific or technical support role (internships,academic projects, or relevant experience are a plus). Technical Skills: Familiarity with scientific software and tools (experience with (Genespring& MPP Software is a plus). Communication Skills: Strong verbal and written communication skills. Ability to explaintechnical concepts in a clear and concise manner. Problem-Solving: Analytical mindset with the ability to troubleshoot complex issues andprovide creative solutions. Team Player: Ability to work effectively in a collaborative team environment and supportboth internal teams and external customers. Adaptability: Willingness to learn and grow in a dynamic, fast-paced environment. Willingness to work in Night shifts.We offer An innovative and open culture in a truly multicultural environment An opportunity to make a fundamental impact on human health Vibrant multidisciplinary scientific interaction and learning opportunity A collaborative and solution-oriented environment where you can make a difference A competitive salary and generous benefits

About Strand Life Sciences:Strand is a 24-year-old spin-off from the Indian Institute of Science. We are a cutting-edge Genomicscompany with a global customer base. We build applications that use DNA sequencing to improvehuman health. In the process, we build algorithms, data pipelines, and visualizations to handle largeamounts of sequence data. We are committed to transforming complex data into actionable insights,contributing to groundbreaking research and innovative solutions in the field of genomics. Weanticipate that in the next few years, hundreds of millions of individuals will have their DNA sequenced,and invite you to join us in this transformative journey.About the PositionWe are seeking a highly skilled and experienced Software Engineer with 5+ years of industryexperience to join our dynamic team. The ideal candidate should have a strong background in softwaredevelopment, problem-solving, and the ability to work in a fast-paced environment. You will beresponsible for designing, developing, testing, and maintaining scalable software solutions.Key Responsibilities: Software Development: Design, develop, and maintain high-quality, scalable, and eclient applications. Code Quality: Write clean, maintainable, and well-documented code following bestpractices. Technical Leadership: Mentor junior developers and contribute to code reviews andtechnical discussions. Collaboration: Work closely with cross-functional teams, including product managers,designers, and QA engineers, to deliver robust solutions. Architecture & Design: Contribute to architectural decisions and suggest improvements toenhance system performance. Testing & Debugging: Perform unit testing, integration testing, and debugging to ensurehigh application reliability. Agile Methodology: Participate in agile development processes, including sprint planning,daily stand-ups, and retrospectives. Innovation: Stay updated with emerging technologies and propose innovative solutions toimprove the development process.Required Skills & Qualifications: Education: Bachelors or Masters degree in Computer Science, Software Engineering, or arelated field. Experience: 5+ years of professional software development experience. Programming Languages: Proficiency in Java.` Frameworks & Technologies: Experience with Spring Boot. [Angular, Node.js, and .NET willbe an add-on]. Database Management: Strong knowledge of Snow Flake & Elastic Search is a must. Cloud & DevOps: Familiarity with cloud platforms like AWS, Azure and Google Cloud, andexperience with CI/CD pipelines. Version Control: Proficiency in Git and working with repositories like GitHub andGitLab. Problem-Solving: Strong analytical and debugging skills with a keen attention to detail. Soft Skills: Excellent communication, teamwork, and time-management skills.Preferred Qualifications: Experience in microservices architecture and RESTful API development. Knowledge of containerization and orchestration tools like Docker and Kubernetes. Exposure to AI/ML, data analytics, or cybersecurity would be a plus.We offer An innovative and open culture in a truly multicultural environment An opportunity to make a fundamental impact on human health Vibrant multidisciplinary scientific interaction and learning opportunity A collaborative and solution-oriented environment where you can make a difference A competitive salary and generous benefits