28 Eli Lilly jobs in India

Drug Development Cloud Engineer

Hyderabad, Andhra Pradesh Bristol Myers Squibb

Posted today

Job Viewed

Tap Again To Close

Job Description

Position: Software Engineer I Veeva Quality


Location : Hyderabad, India

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.


Position Summary:

At BMS (Bristol Myers Squibb), digital innovation and Information Technology are central to our vision of transforming patients’ lives through science. To accelerate our ability to serve patients around the world, we must unleash the power of technology. We are committed to being at the forefront of transforming the way medicine is made and delivered by harnessing the power of computer and data science, artificial intelligence, and other technologies to promote scientific discovery, faster decision making, and enhanced patient care.

Software Engineer I role is a member of the Veeva Drug Development & Cloud team and is accountable for Veeva Configuration and Operational activities in the various vaults of the BMS Veeva ecosystem. In this role, the individual is primarily responsible for supporting platform updates, enhancements and/or end-user support & access management activities including Architecture, design, and testing. This role does not have any supervisory responsibility, however, may act as a functional mentor to more junior team members.

If you want an exciting and rewarding career that is meaningful, consider joining our diverse team!


Desired Candidate Characteristics:

  • Have a strong commitment to a career in technology with a passion for healthcare
  • Ability to understand the needs of the business and commitment to deliver the best user experience and adoption
  • Able to collaborate across multiple teams
  • Excellent communication skills
  • Innovative and inquisitive nature to ask questions, offer bold ideas and challenge the status quo
  • Agility to learn new tools and processes


Key Responsibilities:

  • Supporting a wide range of projects across multiple domain areas, selected candidate’s responsibilities will include:
  • Collaborate closely with the Veeva Drug Dev & Quality Cloud team to obtain high level overview knowledge of the Veeva vault platform and various vaults
  • Assist in the deployment of the Veeva Vault Platform and general releases including documentation and testing
  • System analysis, design, and configuration to meet business requirements
  • Contribute to all aspects of testing activities (unit, system, and/or user acceptance testing) of the vault release including script generation, execution, review, and approval
  • Deliver on validation documentation required on the various operational activities to ensure maintenance of the system’s validated state
  • Provide operational support activities of the Veeva vaults to our global user community, such as maintenance and break-fix releases, security assessments, regulatory risk assessments, incident response, etc.
  • Perform periodic user access review of the applications
  • Obtain/maintain a Veeva Associate Administrator Level certification


Qualifications & Experience:

  • Requires thorough knowledge of the principles and concepts of a discipline and developed knowledge of other related disciplines, typically gained through a university degree and 2-3 years of experience.
  • Works within established procedures. Actively participates in troubleshooting of routine problems.
  • Makes decisions that impact own work and other groups/teams.
  • Works under minimal supervision.
  • Does not have any supervisory responsibility, however, may act as a functional mentor to more junior team members.
  • Experience in implementing/supporting SaaS (Software as a Service) solutions
  • Experience in automated testing tools
  • Experience in life science industry with Quality domain knowledge
  • Experience in GMP (Good Manufacturing Practice) practices
  • Makes decisions while understanding the team's work and how it fits into the broader enterprise.
  • May need support from within the team or outside the team when working on broader or complex topics in understanding environment.
  • Identifies opportunities to improve and grow, balancing performance feedback and career development
  • Applies a continuous improvement mindset in enhancing efficiency, quality and effectiveness or their work outputs.
  • Displays understanding of performance metrics driving the team's goals and questions the external environment and its' implication on the goals and strategies.
  • Able to review multiple factors of data and can effectively organize information to compare and assess short and long-term implications.
  • Can create a well-developed recommendation and sound actions.
  • Ideal candidate will also have Veeva Associate Administrator Level (previously called Veeva White Belt) certification.

#HYDIT #LI-Hybrid

This advertiser has chosen not to accept applicants from your region.

Senior Formulation Scientist, Drug Development

440001 Nagpur, Maharashtra ₹100000 Annually WhatJobs

Posted 4 days ago

Job Viewed

Tap Again To Close

Job Description

full-time
Our client is actively seeking a highly skilled and experienced Senior Formulation Scientist to join their cutting-edge, fully remote research and development team. This critical role is at the forefront of pharmaceutical innovation, focusing on the design, development, and optimization of novel drug formulations. The ideal candidate will possess a Ph.D. or Master's degree in Pharmaceutical Sciences, Chemistry, or a related discipline, coupled with a substantial track record in pre-formulation, formulation development, and scale-up activities for various dosage forms. You will be responsible for leading projects from concept to clinical trial readiness, employing advanced scientific principles and state-of-the-art technologies. Key responsibilities include developing robust formulations for small molecules and/or biologics, characterizing drug substances and excipients, and conducting stability studies. This position demands a deep understanding of regulatory requirements (e.g., FDA, EMA), a commitment to rigorous scientific inquiry, and the ability to translate complex scientific data into actionable development plans. The Senior Formulation Scientist will collaborate closely with analytical chemists, process engineers, and other R&D scientists, contributing to the overall drug development pipeline. This is a unique opportunity to work in a remote-first environment, contributing to life-saving medicines while maintaining a flexible work-life balance. Responsibilities:
  • Design and develop stable, efficacious, and bioavailable drug formulations.
  • Conduct pre-formulation studies to understand drug substance properties.
  • Select and evaluate appropriate excipients for formulation development.
  • Perform formulation optimization studies using DoE methodologies.
  • Characterize formulated products using various analytical techniques.
  • Develop and validate analytical methods for formulation assessment.
  • Plan and execute stability studies according to ICH guidelines.
  • Support process development and scale-up activities for manufacturing.
  • Troubleshoot formulation and process-related issues.
  • Stay abreast of the latest advancements in pharmaceutical formulation science and technology.
Qualifications:
  • Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
  • Minimum of 7 years of relevant industry experience in pharmaceutical formulation development.
  • Extensive knowledge of various dosage forms (e.g., oral solid, parenteral, topical).
  • Proficiency in formulation development techniques and characterization methods.
  • Strong understanding of GMP, ICH guidelines, and regulatory submission requirements.
  • Experience with drug substance characterization and solid-state properties.
  • Excellent analytical, problem-solving, and critical thinking skills.
  • Strong written and verbal communication skills.
  • Ability to work independently and manage multiple projects effectively in a remote setting.
  • Experience with biologics formulation is a plus.
This advertiser has chosen not to accept applicants from your region.

Senior Formulation Scientist - Drug Development

380001 Ahmedabad, Gujarat ₹1100000 Annually WhatJobs

Posted 10 days ago

Job Viewed

Tap Again To Close

Job Description

full-time
We are seeking a highly skilled and experienced Senior Formulation Scientist to join our innovative pharmaceutical R&D team in Ahmedabad, Gujarat . The successful candidate will be responsible for the design, development, and optimization of novel drug formulations, focusing on oral dosage forms. This role requires a strong scientific background, hands-on laboratory experience, and a deep understanding of pharmaceutical sciences and regulatory requirements.

Responsibilities:
  • Design and execute pre-formulation studies to characterize drug substances.
  • Develop and optimize formulations for various dosage forms, with a primary focus on oral solids (tablets, capsules).
  • Evaluate and select appropriate excipients to achieve desired drug product performance and stability.
  • Perform laboratory experiments to investigate solubility enhancement, bioavailability improvement, and controlled/sustained release profiles.
  • Utilize analytical techniques (e.g., HPLC, UV-Vis, dissolution testing) for characterization and quality control of formulations.
  • Prepare comprehensive study protocols, reports, and technical documentation for regulatory submissions.
  • Troubleshoot formulation-related challenges and implement effective solutions.
  • Collaborate with analytical development, process development, and regulatory affairs teams.
  • Stay abreast of the latest advancements in formulation technologies and industry best practices.
  • Mentor junior scientists and contribute to the scientific growth of the R&D department.
  • Ensure compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines.
  • Participate in cross-functional project team meetings and contribute to strategic decision-making.
Qualifications:
  • Master's or Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related discipline.
  • Minimum of 5-7 years of hands-on experience in pharmaceutical formulation development, with a focus on oral dosage forms.
  • Proven expertise in formulation design, excipient selection, and drug product characterization.
  • Proficiency in analytical methods for drug substance and drug product characterization.
  • Strong understanding of physicochemical properties, biopharmaceutics, and pharmacokinetics.
  • Experience with various dosage form manufacturing processes and equipment.
  • Knowledge of regulatory requirements for drug development (e.g., ICH guidelines).
  • Excellent problem-solving, analytical, and critical-thinking skills.
  • Strong written and verbal communication skills, with the ability to present scientific data effectively.
  • Ability to work independently and collaboratively in a fast-paced R&D environment.
  • Experience with pre-formulation studies and solid-state characterization techniques.
This hybrid role offers a blend of laboratory-based work and remote responsibilities, contributing to critical drug development projects. Our client is committed to scientific excellence and innovation in bringing life-changing medicines to market.
This advertiser has chosen not to accept applicants from your region.

Senior Formulation Scientist, Drug Development

226001 Lucknow, Uttar Pradesh ₹1100000 Annually WhatJobs

Posted 15 days ago

Job Viewed

Tap Again To Close

Job Description

full-time
Our client, a leading pharmaceutical company, is seeking a talented and experienced Senior Formulation Scientist to drive innovation in drug product development. This hybrid role is crucial for designing, developing, and optimizing pharmaceutical formulations for new and existing drug candidates. You will work at the forefront of pharmaceutical science, translating complex molecular entities into safe, effective, and stable dosage forms. The ideal candidate will possess a deep understanding of pharmaceutical sciences, excipient functionality, and drug delivery systems.

Key Responsibilities:
  • Design and develop robust formulations for various dosage forms (e.g., oral solids, injectables, topical).
  • Conduct pre-formulation studies to characterize drug substances and excipients.
  • Optimize formulations to achieve desired physicochemical properties, bioavailability, and stability.
  • Plan and execute formulation development experiments, including scale-up and technology transfer.
  • Develop and validate analytical methods for the characterization of drug products.
  • Prepare detailed technical reports, formulation development protocols, and regulatory submission documents.
  • Collaborate with cross-functional teams including R&D, analytical development, DMPK, and regulatory affairs.
  • Troubleshoot formulation-related issues and provide solutions to manufacturing challenges.
  • Stay abreast of scientific advancements, new technologies, and regulatory guidelines in pharmaceutical formulation.
  • Manage project timelines and resources effectively.
  • Mentor junior scientists and contribute to their professional development.
  • Conduct literature searches and patent reviews related to formulation development.
Qualifications:
  • Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
  • Minimum of 5-7 years of hands-on experience in pharmaceutical formulation development.
  • Proven expertise in developing various dosage forms and understanding of drug delivery systems.
  • In-depth knowledge of excipient functionality, compatibility, and selection.
  • Experience with analytical techniques used for characterizing drug products (e.g., HPLC, DSC, XRPD).
  • Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements (e.g., ICH guidelines).
  • Excellent problem-solving, analytical, and critical-thinking skills.
  • Strong written and verbal communication skills, with the ability to present complex data clearly.
  • Proficiency in scientific literature databases and formulation software.
  • Ability to work effectively in a collaborative, cross-functional team environment.
  • Experience with stability studies and data interpretation.
  • Demonstrated ability to manage projects and meet deadlines.
This is an exciting opportunity to contribute to the development of life-changing medicines. Join a dynamic team and make a significant impact on patient health. The position is located in Lucknow, Uttar Pradesh, IN and requires a hybrid work arrangement.
This advertiser has chosen not to accept applicants from your region.

Lead Formulation Scientist - Drug Development

570001 Mysore, Karnataka ₹140000 Annually WhatJobs

Posted 17 days ago

Job Viewed

Tap Again To Close

Job Description

full-time
Our client, a leading pharmaceutical company dedicated to advancing global health, is seeking an experienced Lead Formulation Scientist to join their innovative research and development department in Mysuru, Karnataka, IN . This senior role is pivotal in the development of novel drug delivery systems and the optimization of existing pharmaceutical formulations. The Lead Formulation Scientist will guide the entire formulation development process, from pre-formulation studies to pilot scale-up, ensuring the efficacy, stability, and safety of new drug products. You will collaborate with chemists, analytical scientists, and regulatory affairs specialists to bring life-saving medications to market. This is an exceptional opportunity for a highly skilled formulation expert to lead critical projects and influence the future of pharmaceutical innovation.

Key Responsibilities:
  • Lead the design, development, and optimization of oral solid dosage forms (tablets, capsules) and potentially other dosage forms (e.g., injectables, topicals).
  • Conduct pre-formulation studies to understand drug substance characteristics relevant to formulation development.
  • Develop scientifically sound formulation strategies to improve drug solubility, bioavailability, and patient compliance.
  • Perform experiments to evaluate excipient compatibility, drug-excipient interactions, and critical process parameters.
  • Oversee the scale-up of laboratory-scale formulations to pilot and commercial manufacturing processes.
  • Develop and validate analytical methods for characterizing formulated products.
  • Ensure all formulation activities comply with Good Manufacturing Practices (GMP) and regulatory guidelines.
  • Collaborate with analytical development teams to ensure product quality and stability.
  • Provide technical guidance and mentorship to junior formulation scientists and technicians.
  • Prepare comprehensive development reports, regulatory submission documents (e.g., IND, NDA sections), and scientific presentations.
  • Stay current with advancements in formulation science, drug delivery technologies, and pharmaceutical manufacturing.
  • Troubleshoot formulation and manufacturing issues, providing scientific expertise for resolution.
Qualifications:
  • Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
  • Minimum of 7 years of progressive experience in pharmaceutical formulation development.
  • Proven expertise in oral solid dosage form development, including tablet and capsule manufacturing.
  • Strong understanding of drug substance characterization, excipient functionality, and manufacturing processes.
  • Experience with pre-formulation techniques, solubility enhancement, and controlled/sustained release technologies.
  • Familiarity with analytical techniques used for drug product characterization (e.g., HPLC, dissolution testing, DSC).
  • Knowledge of GMP regulations and experience preparing regulatory documentation.
  • Excellent problem-solving, critical thinking, and experimental design skills.
  • Strong leadership, project management, and communication abilities.
  • Ability to work effectively in a cross-functional team environment.
  • Experience with statistical analysis and design of experiments (DoE) is a plus.
Join our client's esteemed pharmaceutical team in Mysuru and play a vital role in developing innovative medicines.
This advertiser has chosen not to accept applicants from your region.

Senior Formulation Scientist - Drug Development

500001 Hyderabad, Andhra Pradesh ₹1000000 Annually WhatJobs

Posted 18 days ago

Job Viewed

Tap Again To Close

Job Description

full-time
Our client, a leading pharmaceutical company, is seeking an experienced Senior Formulation Scientist to join their innovative Research and Development division. This role, based in **Hyderabad, Telangana, IN**, is integral to the development of novel drug delivery systems and optimizing the formulation of new chemical entities (NCEs) and generic drugs. You will be responsible for designing, executing, and documenting pre-formulation studies, formulation development, and process optimization for various dosage forms. Responsibilities include: Designing and conducting pre-formulation studies to characterize drug substances. Developing robust and scalable formulations for oral, parenteral, topical, and other dosage forms. Performing stability studies according to ICH guidelines. Optimizing formulation processes and excipient selection. Troubleshooting formulation challenges and scale-up issues. Collaborating with analytical development, DMPK, and regulatory affairs teams. Preparing technical reports, study protocols, and CMC documentation for regulatory submissions. Staying current with scientific literature, industry trends, and new technologies in pharmaceutical formulation. Mentoring junior scientists and contributing to a culture of scientific excellence. The ideal candidate holds a Master's or Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field. A minimum of 5-7 years of hands-on experience in pharmaceutical formulation development is required. Strong knowledge of various dosage forms (e.g., tablets, capsules, injectables, topical preparations) and their manufacturing processes is essential. Experience with formulation development for NCEs and generics is highly desirable. Proficiency in relevant laboratory techniques and analytical instrumentation is required. Excellent problem-solving, critical thinking, and communication skills are necessary. This hybrid role offers the opportunity to work in a state-of-the-art facility and contribute to the advancement of life-saving medications.
This advertiser has chosen not to accept applicants from your region.

Senior Formulation Scientist - Drug Development

302001 Jaipur, Rajasthan ₹1300000 Annually WhatJobs

Posted 18 days ago

Job Viewed

Tap Again To Close

Job Description

full-time
Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking a highly skilled Senior Formulation Scientist to join their Drug Development team. This role is central to the development of innovative drug formulations, ensuring the efficacy, safety, and stability of new therapeutic products. The ideal candidate will possess extensive experience in pharmaceutical formulation science, including solid dosage forms, sterile products, or parenteral formulations, along with a deep understanding of pre-formulation, formulation development, and scale-up processes. You will lead formulation projects, collaborate with cross-functional teams, and contribute to regulatory submissions. This position requires a strong scientific background, excellent problem-solving abilities, and a commitment to pharmaceutical quality standards.

Key Responsibilities:
  • Lead the design, development, and optimization of novel drug formulations for various dosage forms (e.g., tablets, capsules, injectables, topicals).
  • Conduct pre-formulation studies to characterize drug substances and excipients.
  • Develop and validate robust formulation and manufacturing processes.
  • Perform stability studies and interpret data to assess product shelf-life.
  • Troubleshoot formulation-related issues and propose effective solutions.
  • Collaborate closely with analytical development, DMPK, and manufacturing teams.
  • Prepare scientific reports, technical documentation, and contribute to regulatory submissions (e.g., IND, NDA).
  • Stay abreast of the latest advancements in formulation science and pharmaceutical technology.
  • Supervise and mentor junior scientists and research associates.
  • Manage project timelines and deliverables effectively.
  • Ensure adherence to cGMP guidelines and quality standards throughout the development process.
  • Evaluate new excipients and drug delivery technologies.

Qualifications:
  • Master's degree or Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
  • Minimum of 5 years of experience in pharmaceutical formulation development.
  • Hands-on experience with various dosage forms and formulation techniques.
  • Proficiency in pre-formulation characterization and drug delivery systems.
  • Strong understanding of physical chemistry, materials science, and analytical techniques.
  • Experience with scale-up and technology transfer activities.
  • Excellent problem-solving, analytical, and critical thinking skills.
  • Strong written and verbal communication skills, with the ability to present scientific data.
  • Knowledge of regulatory requirements (e.g., FDA, EMA) related to drug product development.
  • Experience in a hybrid work environment is beneficial.
This role is a fantastic opportunity for an experienced formulation scientist to make a significant impact in pharmaceutical innovation.
This advertiser has chosen not to accept applicants from your region.
Be The First To Know

About the latest Eli lilly Jobs in India !

Remote Clinical Research Scientist - Drug Development

110001 Delhi, Delhi ₹1600000 Annually WhatJobs

Posted 12 days ago

Job Viewed

Tap Again To Close

Job Description

full-time
Our client, a leading pharmaceutical innovator, is seeking a highly skilled and motivated Remote Clinical Research Scientist to contribute to their cutting-edge drug development programs, supporting research remotely from **Delhi, Delhi, IN**. This critical role involves the design, execution, and monitoring of clinical trials, ensuring adherence to regulatory guidelines and scientific rigor. You will be responsible for developing clinical trial protocols, investigator brochures, and case report forms (CRFs). A deep understanding of pharmaceutical sciences, pharmacology, and clinical trial methodologies is essential. You will collaborate with cross-functional teams, including regulatory affairs, biostatistics, data management, and clinical operations, to ensure seamless trial progression. Data analysis and interpretation of clinical trial results, including the preparation of study reports and publications, will be a key responsibility. You will stay abreast of the latest scientific literature and emerging trends in relevant therapeutic areas. The ideal candidate will possess strong analytical and problem-solving skills, with the ability to critically evaluate scientific data and make informed decisions. Excellent written and verbal communication skills are paramount for effective scientific discourse and reporting. This position is fully remote, offering a flexible work environment while demanding high levels of productivity and accountability. You will contribute to the strategic planning of clinical development programs and provide scientific input into regulatory submissions. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is required. A Ph.D. or Master's degree in a relevant life science discipline (e.g., Pharmacy, Pharmacology, Biotechnology) is mandatory. Previous experience in clinical research within the pharmaceutical or biotechnology industry is essential. This is an exceptional opportunity to advance novel therapies and make a significant impact on patient health, working remotely from **Delhi, Delhi, IN**.
This advertiser has chosen not to accept applicants from your region.

Lead Research Scientist - Oncology Drug Development

302001 Jaipur, Rajasthan ₹150000 Annually WhatJobs

Posted 15 days ago

Job Viewed

Tap Again To Close

Job Description

full-time
Our client is seeking a highly motivated and accomplished Lead Research Scientist to join their cutting-edge pharmaceutical research team, operating on a fully remote basis. This role is crucial for driving innovation in oncology drug discovery and development. You will be instrumental in designing and executing complex research projects aimed at identifying novel therapeutic targets and developing first-in-class small molecule or biologic drugs for various cancer types. This position requires a deep understanding of cancer biology, molecular pharmacology, and drug discovery pipelines.

Key responsibilities include:
  • Designing and overseeing preclinical research strategies for oncology therapeutics.
  • Leading a team of scientists in hypothesis-driven research and experimental design.
  • Analyzing and interpreting complex biological data to guide project direction.
  • Developing and validating in vitro and in vivo models for drug efficacy and safety testing.
  • Collaborating closely with cross-functional teams including medicinal chemistry, DMPK, and translational science.
  • Identifying and evaluating external research collaborations and technologies.
  • Staying abreast of the latest scientific advancements and competitive landscape in oncology.
  • Preparing and presenting research findings at internal meetings and external scientific conferences.
  • Contributing to the preparation of regulatory documents and patent applications.
  • Mentoring and guiding junior researchers.

The successful candidate will hold a Ph.D. in Molecular Biology, Pharmacology, Biochemistry, or a related field, with a minimum of 7 years of post-doctoral or industry experience in cancer research and drug discovery. A strong publication record and proven success in leading research projects from discovery to preclinical development are essential. Expertise in cancer genomics, immunology, or specific signaling pathways relevant to oncology is highly desirable. Excellent analytical, problem-solving, and communication skills are paramount for this remote role, requiring the ability to collaborate effectively across geographical boundaries. This is a unique opportunity to significantly contribute to the development of life-saving cancer treatments within a dynamic and forward-thinking organization.
This advertiser has chosen not to accept applicants from your region.

Senior Clinical Research Scientist - Remote Drug Development

390007 Vadodara, Gujarat ₹120000 Annually WhatJobs

Posted today

Job Viewed

Tap Again To Close

Job Description

full-time
Our client is seeking a highly experienced Senior Clinical Research Scientist to join their fully remote drug development team. This is a critical role focused on designing, implementing, and monitoring clinical trials for novel pharmaceutical compounds. You will be responsible for developing clinical protocols, analyzing trial data, and ensuring compliance with regulatory guidelines and ethical standards. This position requires a deep understanding of clinical trial methodologies, pharmacology, and disease pathophysiology.

The ideal candidate will possess a strong scientific background, with a proven track record in pharmaceutical research and development. You will be adept at translating scientific findings into actionable clinical research plans and communicating complex scientific information effectively to diverse audiences, including regulatory agencies, investigators, and internal stakeholders. This role demands excellent analytical, problem-solving, and critical thinking skills.

Key responsibilities include providing scientific leadership for clinical development programs, authoring study protocols and clinical study reports, and interpreting clinical data to assess drug efficacy and safety. You will collaborate closely with cross-functional teams, including biostatistics, data management, regulatory affairs, and medical affairs, to ensure successful trial execution. Staying abreast of the latest scientific advancements and regulatory changes in the pharmaceutical industry is essential.

We are looking for a self-motivated and results-oriented individual who can work independently and manage multiple projects concurrently in a remote setting. Excellent written and verbal communication skills are paramount. This is an exceptional opportunity to contribute to the development of life-saving medicines and advance your career in pharmaceutical research from anywhere.

**Responsibilities:***
  • Design and develop clinical trial protocols for new drug candidates.
  • Oversee the conduct of clinical trials, ensuring adherence to protocols and regulations.
  • Analyze and interpret clinical trial data to assess safety and efficacy.
  • Author study reports, manuscripts, and regulatory submission documents.
  • Collaborate with internal and external stakeholders on clinical development strategies.
  • Provide scientific expertise and guidance to project teams.
  • Stay current with scientific literature and regulatory guidelines.
**Qualifications:***
  • Ph.D. or M.D. in a relevant life science discipline.
  • Minimum 8 years of experience in clinical research within the pharmaceutical industry.
  • Demonstrated experience in designing and managing Phase I-IV clinical trials.
  • In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Strong analytical and statistical interpretation skills.
  • Excellent written and verbal communication abilities.
  • Proven ability to work effectively in a remote, collaborative environment.
Contribute to groundbreaking pharmaceutical research from your home base, impacting global health outcomes.
This advertiser has chosen not to accept applicants from your region.
 

Nearby Locations

Other Jobs Near Me

Industry

  1. request_quote Accounting
  2. work Administrative
  3. eco Agriculture Forestry
  4. smart_toy AI & Emerging Technologies
  5. school Apprenticeships & Trainee
  6. apartment Architecture
  7. palette Arts & Entertainment
  8. directions_car Automotive
  9. flight_takeoff Aviation
  10. account_balance Banking & Finance
  11. local_florist Beauty & Wellness
  12. restaurant Catering
  13. volunteer_activism Charity & Voluntary
  14. science Chemical Engineering
  15. child_friendly Childcare
  16. foundation Civil Engineering
  17. clean_hands Cleaning & Sanitation
  18. diversity_3 Community & Social Care
  19. construction Construction
  20. brush Creative & Digital
  21. currency_bitcoin Crypto & Blockchain
  22. support_agent Customer Service & Helpdesk
  23. medical_services Dental
  24. medical_services Driving & Transport
  25. medical_services E Commerce & Social Media
  26. school Education & Teaching
  27. electrical_services Electrical Engineering
  28. bolt Energy
  29. local_mall Fmcg
  30. gavel Government & Non Profit
  31. emoji_events Graduate
  32. health_and_safety Healthcare
  33. beach_access Hospitality & Tourism
  34. groups Human Resources
  35. precision_manufacturing Industrial Engineering
  36. security Information Security
  37. handyman Installation & Maintenance
  38. policy Insurance
  39. code IT & Software
  40. gavel Legal
  41. sports_soccer Leisure & Sports
  42. inventory_2 Logistics & Warehousing
  43. supervisor_account Management
  44. supervisor_account Management Consultancy
  45. supervisor_account Manufacturing & Production
  46. campaign Marketing
  47. build Mechanical Engineering
  48. perm_media Media & PR
  49. local_hospital Medical
  50. local_hospital Military & Public Safety
  51. local_hospital Mining
  52. medical_services Nursing
  53. local_gas_station Oil & Gas
  54. biotech Pharmaceutical
  55. checklist_rtl Project Management
  56. shopping_bag Purchasing
  57. home_work Real Estate
  58. person_search Recruitment Consultancy
  59. store Retail
  60. point_of_sale Sales
  61. science Scientific Research & Development
  62. wifi Telecoms
  63. psychology Therapy
  64. pets Veterinary
View All Eli Lilly Jobs