26 Lifesciences Jobs

As a Strategic Account Manager at SCIEX, you will play a pivotal role in influencing life-changing research outcomes and accelerating your potential within the life sciences, diagnostics, and biotechnology industry. You will be a part of a winning team that is passionate about empowering life science experts worldwide to solve impactful analytical challenges through innovation and reliability. Key Responsibilities: - Work collaboratively with a team to achieve annual sales goals and increase market share by establishing and nurturing strong relationships with key decision makers in assigned Strategic Accounts. - Serve as the primary point of contact for strategic accounts, coordinating inter...

Your key responsibilities include managing multiple, large and complex global regulatory submission projects, developing and providing submission and contributing to the technical related regulatory strategy, intelligence and knowledge required to develop, register, and maintain global products. You will also contribute to strategic and technical input/support to drive implementation of global systems, tools and processes to support global development projects and/or marketed products. As a seasoned, experienced professional with a full understanding of your area of specialization, you will resolve a wide range of issues in creative ways. This job is a fully qualified, career-oriented, journ...

The Associate Medical Expert in Translational Clinical Oncology (TCO) serves as the medical leader for global, roll-over, and long-term follow-up studies, as well as studies in the close-out phase. Additionally, they provide medical support for assigned components of active TCO studies under the guidance of a Clinical Program Leader (CPL) or Medical Expert. TCO, a department within the Biomedical Research division, specializes in designing and conducting early-phase clinical studies in cancer patients, bridging the gap between drug discovery and late-phase clinical development to deliver innovative oncology treatments. In this role, your major responsibilities include providing medical suppo...

Major accountabilities: Provides medical support to Clinical Program Leader (CPL) leading the program. Medical support may include, but is not limited to, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents such as Investigator Brochures, responses to Health Authority questions and conducting ongoing review of clinical trial data, with oversight of TCO deliverables. May act as the medical monitor to support overall program safety reporting (e.g., Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety Team. May represents CPL at project team meetings (e.g. CTT) and may pro...

Career Institute of Medical Sciences is a 150+ Bedded Multi Specialty Health Care Centre in Bhopal, Madhya Pradesh, that provides services related to General Medicine, Plastic Surgery, General & Laparoscopic Surgery, Dentistry, Cardiology, ENT, Ophthalmology, Orthopaedics, Paediatrics, Obstetrics and Gynaecology, Urology, Neurosciences including Neurology and neurosurgery, Dermatology, Pathology & Radiology. We provide complete services for treatment of emergency, acute and follow up care for patients of all age groups. We are looking for a dedicated and compassionate General Physician to join our healthcare team in Bhopal. The ideal candidate will provide comprehensive medical care to patie...

Summary Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place to classify and maintain records. Interprets & enforces all documentation formatting, standards, policies, and operating procedure requirements. May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers. May analyze and evaluate data, extract pertinent information, prepare informatio...

The GCP Compliance Manager (GCO) is responsible for overseeing and controlling compliance of regulated GCO activities, focusing on those with a high impact on GCO's ability to meet objectives. This role plays a crucial part in supporting GCP Compliance pillars, including issue management, audits, and inspections, particularly system/process audits and global inspections for authorizations and GCO self-strategy delivery. As the GCP Compliance Manager (GCO), you will provide GxP expertise and support GCP Compliance for various functions, compliance, process, training, and risk groups. Your responsibilities will include managing systemic quality issues, deviations, quality events, audits, and i...

You will be working as a Proposal Writer in the Presales team at Xybion's Chennai location. Your primary responsibilities will include reviewing and analyzing RFPs and RFIs to understand product and service requirements, managing the proposal development process, interpreting detailed requirements, and creating concise, well-written proposals that are compliant and aligned with the company's value proposition. As a Proposal Writer, you will collaborate with various stakeholders such as SMEs, Technical Architects, and Product Specialists to craft compelling bid solution responses. It is essential to be detail-oriented, prioritize responsibilities to meet deadlines, and maintain version contro...

You will be responsible for executing cell-based assays on nutraceuticals for human diseases in R&D labs located in Rabale, Navi Mumbai. During the training period at Chunabhatti, Mumbai, you will be expected to demonstrate proficiency in M.Sc in Biotechnology and Lifesciences. Your duties will include screening of phytocompounds through cell culture, Western blotting, and RNA experiments. Additionally, you will be assisting in the preparation of manuscripts for international publication, with the opportunity to be credited as an author on papers. You will have the privilege of working in cutting-edge, state-of-the-art laboratory facilities. Candidates residing in Navi Mumbai are preferred f...

The Associate Medical Expert in Translational Clinical Oncology (TCO) plays a crucial role as the medical leader for various global studies, roll-over studies, long-term follow-up studies, and studies in the close-out phase. Working under the guidance of a Clinical Program Leader (CPL) and/or Medical Expert, you will provide essential medical support for assigned aspects of active TCO studies. TCO is a department within the Biomedical Research division that focuses on designing and conducting early phase clinical studies in cancer patients, aiming to develop innovative treatments for oncology conditions and bridge the gap between drug discovery and late-phase clinical development. In this ro...

The Associate Clinical Development Director (Assoc. CDD) plays a crucial role in contributing to the development of protocols for assigned global clinical trials, monitoring scientific aspects, and ensuring the reporting of high-quality data. Depending on the size and complexity, they may also provide support in developing the clinical and scientific strategy for specific sections of a clinical development program. Their responsibilities encompass overseeing all operational aspects of clinical trials, from planning and execution to interpreting research findings and managing data collection activities and clinical operations. Additionally, they are responsible for complete oversight of budge...

As an Associate at ZoomRx, you will be part of a rapidly growing life science market research and consulting company that focuses on the intersection of data, healthcare, and technology. We assist leading biopharmaceutical companies in answering unique questions and provide market intelligence throughout their business lifecycle. Our impactful products include Ferma.AI, PERxCEPT, HCP-PT, and Brand Builder, offering various services such as healthcare intelligence, omnichannel tracking, market insights, and brand optimization. We operate with a flat organizational structure that encourages risk-taking, learning from mistakes, and continuous growth towards achieving career goals. You will thri...

Roles and Responsibilities; Provide scientific support for internal teams, marketing, and field medical teams Prepare scientific documents including slide decks, Q&A documents, clinical summaries, product dossiers, and white papers Review promotional and medical materials for scientific accuracy and compliance Stay up to date with the latest scientific literature and product-related publications Collaborate with Medical Affairs, Regulatory, and Pharmacovigilance departments Respond to medical information queries from field force and customers Ensure compliance with medical, ethical, and promotional guidelines Eligibility / Qualifications: B.Pharm / M.Pharm / M.Sc. in Life Sciences, Microbiol...

The Marketing Transformation Senior Manager role within Accenture GN Song involves working at the core of the top global Life Sciences industry, including Pharmaceuticals, Biotechnology, and Medical Technology. As a Senior Manager, you will collaborate on innovative projects, leveraging deep industry knowledge and marketing skills. Your responsibilities will encompass strong project management to successfully plan, execute, and deliver content initiatives, while also coordinating cross-functional teams and managing resources effectively. An analytical and data-driven mindset will be crucial in driving result-oriented decisions. Your role will involve providing consulting and advisory service...

The Medical Expert in TCO (Translational Clinical Oncology) serves as the medical leader for assigned global, roll-over, and long-term follow-up studies, as well as studies in the close-out phase. Additionally, they may provide medical co-leadership for assigned aspects of global, active TCO studies under the guidance of a Clinical Program Leader (CPL). TCO, a department under the Biomedical Research division, is responsible for designing and conducting early-phase clinical studies in cancer patients, acting as a connection between drug discovery and late-phase clinical development to deliver innovative medicines for oncology conditions. Responsibilities include providing medical support to ...

Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place to classify and maintain records. Interprets and enforces all documentation formatting, standards, policies, and operating procedure requirements. May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers. May analyze and evaluate data, extract pertinent information, prepare information abst...

Lead South Asia Lifesciences sales team Develop new buss for Pharma & Nutrition Excipients Handle pricing & supply related matters at customer end Deliver revenue & Gross profit targets for Lifesciences Buss Manage & coordinate customer TSR Required Candidate profile Strong understanding of KAM Buss acumen with knowledge of local commercial matters Ability to prioritize with proven planning & organizational skills Able to conceptualize & promote ideas effectively

About Everest Group Confident decisions driven by deep expertise and tenacious research. Everest Group helps business leaders confidently navigate todays market challenges, driving maximized operational and financial performance and transformative experiences. Our deep expertise and tenacious research focused on technology, business processes, and engineering through the lenses of talent, sustainability, and sourcing delivers precise and action-oriented guidance. For more information, visit www.everestgrp.com. Job Overview This role is part of the BPS Pricing cluster within the Commercial and Solution Analytics (CSA) practice, which assists buyers and service providers with pricing decisions...

We are urgently seeking experienced professionals with hands-on expertise in Veeva Vault CTMS to join our team. The ideal candidate will provide L2/L3 support for Veeva CTMS, assisting with issue resolution, system troubleshooting, and user support across modules such as Site, Study, Subject, and Monitoring. Key Responsibilities: Provide L2/L3 support for Veeva Vault CTMS Troubleshoot and resolve system issues, user queries, and configuration problems Offer functional support across CTMS modules Site, Study, Subject, Monitoring, etc. Collaborate with internal teams and stakeholders to ensure seamless operations and timely resolution of issues Maintain documentation for recurring issues, reso...

Hi, We are hiring for Leading ITES Company for Aggregate Report Writer Profile. Please Apply, We shall call back relevant profiles. Role & responsibilities: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic Aggregate Safety Reports (PBRER, DSUR etc.). To perform comp...

Sales & BD of Excipients for PAN India for Pharma, Lifesciences & Biopharmaceutical Companies Handling existing accounts, obtain orders & develop new accounts Market info on pricing & products & new products Handle rejections & customer complaints Required Candidate profile Min 10 yrs of relevant exp with familiarity about Pharmaceutical product development & manufacturing operations commitment to excellence Self motivated & passionate to value selling Good team player

Hi We are Hiring for the job role of Medical Writer Job Description: Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas. Quality check of the clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, Clinical Summary of Safety, Clinical Summary of Efficacy and Common Technical Document Modules. Initiate start up meetings with the Study Teams related to the creation and development of the clinic...

Role- AGM- International Business development- LATAM; East Europe / Russia CIS Company- A leading Biopharmaceutical Company Location- Bangalore Reporting To- VP- BD Roles and Responsibilities This role requires a dynamic individual with excellent analytical skills, strategic thinking, and the ability to manage complex projects and partnerships across semi-regulated markets, including Emerging Markets Latin America, Europe, . Expertise in sales and marketing within these regions is essential. Develop international business strategies to drive growth in overseas markets. Identify new opportunities for product launches and market expansions. Analyze market trends, competitor activity, and custo...

Hi, We are hiring for Leading ITES Company for Aggregate Report Writer Profile. Please Apply, We shall call back relevant profiles. Role & responsibilities: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic Aggregate Safety Reports (PBRER, DSUR etc.). To perform comp...

Location: Gurugram/Pune/Bengaluru We are looking for a dynamic domain expert in Life Sciences to drive transformational healthcare projects across US and European markets. If you are passionate about digital innovation and cross-functional leadership in the life sciences sector, this role is for you. Your Future Employer: is a leading global business process management company that co-creates innovative, tech-led solutions for Fortune 500 clients across multiple industriesincluding healthcare and life sciences. Responsibilities: Leading and delivering end-to-end life sciences transformation projects for clients across the US and Europe. Collaborating with cross-functional teams to identify a...