3711 Clinical Research Jobs - Page 27

We re on a mission to change the future of clinical research. At Perceptive, we help the biopharmaceutical industry bring medical treatments to the market, faster. Our mission is to change the world but to do this, we need people like you. Apart from job satisfaction, we can offer you: HEALTH: - Medical plan for you and your dependents. - Personal Accident Insurance - Life Insurance - Critical illness cover WEALTH: - Salary structure and Flexi basket - Provident fund of 12% - Gratuity scheme YOURSELF: Internal growth and development programs & trainings Job Summary: As Software Engineer, you will be responsible for collaborating across functions, working to agreed standards, supporting colle...

We re on a mission to change the future of clinical research. At Perceptive, we help the biopharmaceutical industry bring medical treatments to the market, faster. Our mission is to change the world but to do this, we need people like you. Apart from job satisfaction, we can offer you: HEALTH: - Medical plan for you and your dependents. - Personal Accident Insurance - Life Insurance - Critical illness cover WEALTH: - Salary structure and Flexi basket - Provident fund of 12% - Gratuity scheme YOURSELF: Internal growth and development programs & trainings Job Summary: As Software Engineer, you will be responsible for collaborating across functions, working to agreed standards, supporting colle...

Overview T This role will assist an R&D GBS Technical Market Analysis team based out of Hyderabad and be responsible for conducting scientific, competitive, market, and desk research, consumer testing, and new idea feasibility analysis. This role will support the overall Technical Market Analysis capability by coordinating with in-market teams as required for the provision of accurate and relevant research outputs. Responsibilities Identifies and defines the objective of a research project and determines the best methods to use to meet those objectives. Perform market analysis, consumer needs identification, and consumer / product / desk research and testing activities in line with global re...

Senior Medical Writer (CSR, IB, Protocol Drafting) Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives we re able to create a place...

The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product s safety profile as well as other products within the same therapeutic area. Also, this position plays a greater role as a senior technical leader and participate in matrix management activities including preparation or participation in evaluating safety issues and preparation of aggregate reports in collaboration with the Post-Marketing Safety Experts and Safety Surveillance Group and be responsible for sur...

Provides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions. Assists in the development of detailed documentation and specifications. Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions. Assists in the design and structure of presentations that are appropriate to the characteristics or needs of th...

a meaningful impact on healthcare. Who we re looking for: You will be part of a growing team of engineers located across the world, focused on building new and modern software that s positioned to disrupt the clinical trial space. In this remote role, you ll be empowered and encouraged to think outside the box to develop innovative solutions to drive business and the industry forward. Not only do you love to code, but you are also a self-motivated individual who can apply strong critical thinking and problem-solving skills to daily challenges. You re ultimately a JavaScript/TypeScript aficionado but also enjoy wearing many different hats. Position overview: We re seeing immense growth in the...

About You Experience, Education, Skills, and Accomplishments Masters degree in Epidemiology or Public Health Atleast 3 years of Systematic literature review experience A strong methodological background in epidemiology Familiar with MS Office including MS Word, Power Point, and Excel. It would be great if you also have Experience with client interaction Experience analyzing large data sets Claims data analysis experience in SQL and/or Python Oncology experience RWD and SAS experience About the Team We are a global team approximately 40+ team members located across U.S. Canada and India, specialized in Epidemiology. Work hours Monday to Friday (Hybrid work model) 12PM 9 PM

Job Description: Job Title: Regulatory Filtering Analyst Corporate Title: NCT Location: Bangalore, India Role Description Regulatory Operations is responsible for defining and implementing procedures which provide regulatory operations services for various divisions of the bank and its group entities. This is to support the bank in its efforts to ensure regulatory compliance. Work includes: Partnering with the banks regulatory team to translate regulation into operational processes/procedures assisted Developing the banks information technology infrastructure Developing and implementing regulatory strategies, procedures and controls for new products and/or business activities that require go...

Drug Safety Physician We are currently seeking a Drug Safety Physician to join our diverse and dynamic team. As a Drug Safety Physician at ICON, you will play a pivotal role in overseeing the medical aspects of pharmacovigilance activities, ensuring the safety of investigational drugs and contributing to the advancement of inNvative treatments and therapies. What you will be doing Review of coding (e.g. MedDRA) and accurate assessment (seriousness, expectedness, listedness, relatedness) of Adverse Events (serious and non-serious) and of Adverse Drug Reactions (serious and non-serious) Provide support to the Drug Information & Pharmacovigilance Product Support (call) Centre and the related pr...

Company Description Skylimit Research Private Limited provides a comprehensive range of clinical, preclinical, and bio/analytical services supporting innovator, biosimilar, and generic drug development programs globally. As an independent, investor-owned, and professionally managed contract research group, we offer scientific leadership, robust quality management systems, and long-term stability. We serve clients in the clinical research organisation Clinical trial management, Preclinical Research and Development, Regulatory support and submissions of study data, Bioanalytical services, Pharmacovigilance, Statistical Services. Role Description This is a full-time on-site role for a Medical W...

Job Overview The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product s safety profile as well as other products within the same therapeutic area. Also, this position plays a greater role as a senior technical leader and participate in matrix management activities including preparation or participation in evaluating safety issues and preparation of aggregate reports in collaboration with the Post-Marketing Safety Experts and Safety Surveillance Group and be respon...

Job Location: Bangalore Department: Medical Writing About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time t...

Provides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions. Assists in the development of detailed documentation and specifications. Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions. Assists in the design and structure of presentations that are appropriate to the characteristics or needs of th...

About the Opportunity Job Type: PermanentApplication Deadline: 13 September 2025 Title Senior Associate - CASS Governance Department CASS & Oversight Location Gurugram/Kingswood Reports To Associate Director, CASS Governance Level Grade 3 About your team CASS & Oversight function is responsible for compliance with CASS rules across the organisation. The team records breaches in conjunction with Compliance to reduce the risk of loss of client money and assets due to negligence, inadequate reconciliation procedures or administration errors. CASS Specialist Team also submits Client Money & Asset Returns to the regulator on monthly basis. The function also facilitates and manages internal and ex...

Overview T This role will assist an R&D GBS Technical Market Analysis team based out of Hyderabad and be responsible for conducting scientific, competitive, market, and desk research, consumer testing, and new idea feasibility analysis. This role will support the overall Technical Market Analysis capability by coordinating with in-market teams as required for the provision of accurate and relevant research outputs. Responsibilities Identifies and defines the objective of a research project and determines the best methods to use to meet those objectives. Perform market analysis, consumer needs identification, and consumer / product / desk research and testing activities in line with global re...

We are hiring Trainers/ Faculty/ Lecturer for our Pune branch to teach topics clinical research, medical coding, drug discovery Pharmacovigilance. Contact 9856963895 Eligibility : Msc(microbiology), Bpharm, Mpharm, Pharm D

Hiring for Statistical Programmers with strong experience in end-to-end programming ( SDTM, ADaM, TLF ) for a leading Clinical Research organistaion. Location: Remote Role & responsibilities Title: Senior Statistical Programmer Experience: 6+ years Skills Required: Technical: R (expert), Python (proficient), SQL (proficient), experience in IHD software Experience in RWD , mainly in Pharmacology and Epidemiology (post-marketing) Hands-on experience with Real World Databases Optum, Marketscan, Flatiron, JMDC Familiarity with AI/ML, Data Visualization, and reporting tools to apply share Resumes with Puja.k@maxisclinical.com Regards Puja Khemchandani

About You Education (BPharm/MPharm/MSc in Biotechnology, Microbiology, Lifesciences) Minimum 2 years of experience inanalyzing and updating clinical reports In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases Excellent English written and verbal communication skills. It would be great if you also had . . . Experience in secondary research related to clinical information Ability to delve deep into content and results. What will you be doing in this role? Actively seek out information about Clinical trials, analyze, cross reference, and update all new or previously updated information in the Clinical trials records from various sources, w...

Role Description Regulatory Operations is responsible for defining and implementing procedures which provide regulatory operations services for various divisions of the bank and its group entities. This is to support the bank in its efforts to ensure regulatory compliance. Work includes: Partnering with the banks regulatory team to translate regulation into operational processes/procedures assisted Developing the banks information technology infrastructure Developing and implementing regulatory strategies, procedures and controls for new products and/or business activities that require governmental approvals Preparing and submitting regulatory applications such as permits, licenses, certific...

Role Description About Our Engineers Our Engineers work on a diverse range of solutions using cutting-edge technology every day, including our award-winning platforms like Autobahn, Fabric, Glue, and more. Our Technology strategy is designed to build new revenue streams and develop innovative ideas which produce a new competitive advantage for the Bank, whilst also fixing our foundations and focusing on the importance of stability and risk management. Corporate Bank Technology understands the clients needs and has a robust strategy and innovative approach to deliver. About the Team Cash Management Payment Orchestration : Cash Management Payment Orchestration has an end-to-end responsibility ...

About The Role Skill required: AML fraud mgmt. Financial Crime & Fraud Management Designation: Regulatory Compliance Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years What would you do? Investigate Fraud and Disputes, review and determine the request and validate the chargeback.Looking for someone with AML and Fraud mgmt experience.Strategize, architect, Analyse, design, implement and contribute to engagements involving tools and processes associated with the prevention (or management ) of fraud. What are we looking for? Written and verbal communicationEnd to end knowledge in the areas of Fraud investigation, Fraud Detection, Dispute & Chargebacks.Understanding of Re...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: BCom Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving customer iden...

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical data SVS Analyst Qualifications: Any Graduation,BE,MCA Years of Experience: 3-5 Yrs What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around...

About The Role Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Associate Qualifications: BCom Years of Experience: 1 to 3 years Language - Ability: English(Domestic) - Intermediate What would you do? We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade ...