911 Biostatistics Jobs - Page 14

Description Statistical Programmer I Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, inno...

Develop Medical Devices Algorithm, Test Medical Devices , Clinical Trials, Patient Monitoring, FDA Applications, CE Certifications, ISO Certifications. Perform testing, calibration, troubleshooting, and repair of medical electronic equipment. Collaborate with cross-functional teams including R&D, manufacturing, quality assurance, and clinical staff to ensure product safety and effectiveness. Ensure compliance with medical device regulations and standards (e.g., FDA, IEC 60601, ISO 13485).

We are looking for a highly skilled and experienced Biomedical - Medical Electronics Engineers with 2-4 years of experience to join our team at AARMS Value Chain Pvt. Ltd., located in the Medical Devices & Equipment industry. Roles and Responsibility Develop medical devices algorithms and test them. Conduct clinical trials and monitor patients. Prepare FDA applications and obtain CE certifications. Ensure ISO certifications for medical devices. Collaborate with cross-functional teams to achieve project goals. Analyze data and provide insights to improve product quality. Job Requirements Minimum 2 years of experience in biomedical engineering or medical electronics. Strong knowledge of medica...

Description Biostatistician I Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating ...

Description Medical Writer I Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating a...

As a Geospatial Statistician and Analyst at your company, you will play a crucial role in supporting various geospatial activities and initiatives. Your expertise and skills will contribute to addressing geographic disparities in heart disease and stroke morbidity, mortality, risk factors, and prevention efforts. - Analyze spatial and spatio-temporal data - Manage large datasets - Utilize statistical software such as SAS, R, or GeoDa To excel in this role, you must hold a minimum of a Master's Degree in Statistics, Biostatistics, Epidemiology, Sociology, or Applied Mathematics. Pursuing or possessing a PhD in any of these fields would be advantageous. Your daily tasks will involve providing ...

Summary Of Responsibilities Perform the role of the Lead Statistical Programmer. Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc. Develop and maintain SAS programs to create complete SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs. Produce Define XML/PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs. Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets and contribute to the development of Fortrea and Client ...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function Data Analytics & Computational Sciences Job Sub Function Biostatistics Job Category Scientific/Technology All Job Posting Locations: Bangalore, Karnataka, India...

Title : PYTHON AI ENGINEER - Automated Test Data Generation Location: Remote (India) Timing: 06:30 PM to 03:30 PM IST Overview We are seeking a Python AI Engineer with expertise in synthetic and automated test data generation to support clinical trials, regulatory submissions, and GxP-compliant systems across the life sciences domain. This role will focus on building intelligent frameworks that generate high-quality, audit-ready datasets for use in clinical data management (CDM), biostatistics, pharmacovigilance, and regulatory validation environments. By leveraging AI/ML techniques and Python-based automation, this role will help reduce dependency on production data, accelerate testing cycl...

Your Role We are seeking an experienced and collaborative Senior Statistician I to provide advanced statistical expertise and leadership in support of clinical research studies. This role involves working closely with Biostatisticians, Statistical Programmers, Clinical Data Managers, and sponsor teams to ensure the accuracy, reliability, and regulatory compliance of statistical deliverables. The Senior Statistician will also oversee quality control processes and contribute to the development of statistical analysis plans and datasets. In this role, you will: Provide statistical leadership and support for clinical trials, ensuring high-quality deliverables. Participate in cross-functional stu...

Role Overview: You will be joining Astellas Pharma Inc., a global pharmaceutical company committed to developing innovative therapies for patients worldwide. As a Central Monitor at Astellas Global Capability Centres, you will play a crucial role in supporting drug development projects and ensuring the implementation of Risk Based Quality Management (RBQM) strategies. Your responsibilities will include collaborating with cross-functional study teams, conducting central monitoring activities, and overseeing the documentation and resolution of findings. Your expertise and leadership will contribute to the success of clinical trials and the advancement of medical solutions for patients. Key Res...

Hello Applicant, We are #hiring for Project Technical Support III ! Government Department Payroll company: - E Solutions Job role: - Project Technical Support III ! Educational Qualification :- * B. Sc. (Statistics) (Biostatistics) + three years experience Or * M. Sc. (Statistics, Biostatistics) & Knowledge of SPSS & STATA software Project Name :- A Case Control Study Assessing the Factors Influencing Disability and Mental Health Among Leprosy Patients Visiting Tertiary Care Facilities in Uttar Pradesh, India" Salary :- 28000 /- + HRA Per Month Work Location :- Dr, M. Miyazaki Marg, Forest Colony, Tajganj, Agra, Uttar Pradesh 282001 No. of Vacancy :- 1

Position : Report Writer Department : Biopharmaceutics Department Minimum Experience Required : 3-5 Years Qualification : B.Pharm/M.Pharm/Pharm D Key Responsibilities Prepare and review Clinical Study Reports (CSRs) for Bioequivalence and Phase 1 studies in compliance with global regulatory guidelines, internal SOPs, and client requirements. Analyze and interpret clinical and statistical data with a clear understanding of study results. subject safety narratives and ensure accurate and timely compilation of final CSR packages. Ensure all documents adhere to standards of grammar, formatting, structure, and consistency. Prepare regulatory-compliant appendices for eCTD submissions, including re...

**Greetings from You & I Consulting!** We've proudly helped candidates build careers at 64+ top MNCs across India, and were excited to bring you a new opportunity with a leading global company. If you have experience in Statistical Programming, this role is your next step forward! Senior Lead Statistical Programmer!!! We are hiring for: Senior Lead Statistical Programmer up to 22LPA ctc **To Apply Call on Puja- 8167854231 /Or Whatsapp on the same Number with your CV** Experience Level: 4 to 18 years Location-Mumbai , Kochi, Bangalore and PAN India Job Description : We are seeking an experienced and driven Senior Lead Statistical Programmer with 1015 years of experience in clinical trial prog...

Job Profile: UAT Tester - CTMS & CDM applications Location: Hyderabad Notice period: immediate to 60 days Mandatory Requirements: Clinical Systems, Safety Systems, 21 CFR part 11, GAMP 5, ICH, EMEA, MHRA regulations Roles and Responsibilities Must Have 4 to 8+ years of experience in IT testing/validation, with 2–4+ years in clinical trial systems. Collaborate with Clinical Operations, Data Management, Biostatistics, and IT teams to gather UAT requirements. Develop UAT strategy, test plans, test cases, and traceability matrices mapped to URS (User Requirements). Execute UAT test scripts for CTMS, EDC, eTMF, IRT/IWRS, eCOA/ePRO, and integrations with Safety and Regulatory systems. Validate wor...

Kenvue is currently recruiting for a: Principal Statistical Programmer What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means...

Job description The Medical Writer will be responsible for preparing high-quality clinical, regulatory, and scientific documents that support drug development and regulatory submissions. Experience : 1+ years Location : Hyderabad (Work from office) Roles & Responsibilities: Draft, review, and finalize clinical study protocols, investigator brochures, informed consent forms, and clinical study reports (CSRs). Prepare regulatory submission documents (CTD modules, IND, NDA, MAA dossiers). Write manuscripts, abstracts, and posters for publication/presentation. Ensure compliance with ICH-GCP, FDA, EMA, CDSCO, and other regulatory authority guidelines. Collaborate with clinical, pharmacovigilance,...

Role Overview: You will be the Senior Program Officer for Health and Medical at Operation Blessing India. Your role involves providing leadership to the project, establishing relationships with relevant organizations and stakeholders, and ensuring the smooth implementation of program activities while upholding high standards of integrity. Your responsibilities will include community mobilization, assessment, planning, implementation, reporting, networking, and resource mobilization. Key Responsibilities: - Monitor the implementation of program activities closely - Ensure optimal and timely utilization of resources - Maintain high standards of integrity - Lead community mobilization efforts -...

Job Description Position: Medical Coder Ct: HR HR Shanmugapriya - 8072891550 Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility All (UG/PG) Life Science Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoolo...

Clinical Trial Management, Regulatory Affairs, Data Management & Biostatistics, Medical Writing, Pharmacovigilance & Drug Safety, Preclinical Research, Project Management and Quality Assurance (QA). Candidate should have this basic knowledge: Scientific and clinical knowledge Regulatory and compliance expertise Project and time management Data integrity and attention to detail Cross-functional communication

Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we’re looking for experienced full-time, Hyderabad-based Biostatistician to join us as we prepare to launch of our newest office in Hyderabad, India . This is more than just a job. It’s an opportunity to be part of something from the very beginning. You’ll play a direct role in shaping the culture, building the team, and influencing how we grow in India. From day one, your work will make a meaningful impact across global projects. Why Join Medpace in Hyderabad? Be a Founding Member: Help establish and lead operations at our newest location. Immediate Impact: Your experience will directly influ...

As the Associate Director of Biostatistics at Bristol Myers Squibb, you will be a key member of cross-functional Development teams, contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Your responsibilities may include supporting a particular indication of an asset, developing collaborative relationships, and working effectively with the Biostatistics indication/asset Lead and other cross-functional team members. Key Responsibilities: - Collaborate in the design of innovative and efficient clinical trials, including selecting study population/endpoints and contributing to project development strategy - De...

As a SAS Programmer at Catalyst Clinical Research, you will play a crucial role in providing SAS programming support for Statistics and Data Management functions related to clinical trials and regulatory submissions. Your responsibilities will involve collaborating closely with Biostatisticians and Data Managers to develop SAS programs for validating tables, listings, and figures, as well as assisting with data cleaning and query generation. Additionally, you will serve as a contact for programming activities within the organization. Key Responsibilities: - Perform data manipulation techniques and advanced programming techniques such as arrays, transpositions, complex merges, SQL, SDTM, etc....

About The Job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main Responsibilities The Principal Biostatistician will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans (SAP), programming specifications for a...

About the job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main responsibilities: The Principal Biostatistician will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans (SAP), programming specifications for ...