911 Biostatistics Jobs - Page 17

Job Description Potential candidates should have knowledge in general math modeling, Statistical Modelling (ML) and simulation techniques. Candidates should have hands-on experience in developing quantitative models. They should possess the ability to translate a business problem into an analytical problem, recommend, implement and validate quantitative models, and generate/deliver insights to stakeholders. Preference would be given to candidates that are intellectually curious, innovative thinkers, and have demonstrated ability to solve problems independentl Responsibilities Collaborate with cross-functional teams to understand the business, customer personas and customer pain points, and d...

The University of Hong Kong Apply now Ref.: 532936 Work type: Full-time Department: School of Public Health (22400) Categories: Senior Research Staff & Post-doctoral Fellow Hong Kong Applications are invited for appointment as Post-doctoral Fellow in Epidemiology and Biostatistics in the School of Public Health (Ref.: 532936), to commence as soon as possible on temporary term basis for one or two years, with the possibility of renewal subject to satisfactory performance and funding availability. Applicants should possess a Ph.D. degree in epidemiology or a related discipline, with a strong background in infectious disease epidemiology, surveillance and control. They should have excellent com...

Major accountabilities: Drive the implementation of data analytics reports and dashboards for optimal data review by working with the users to establish robust user specifications and with programmers to implement the optimal output -Translate business requirements into logical models and provide direction to the development team to translate business logic. Lead authoring of the user requirements document, functional specifications and functional testing scripts -Proactively identify or address needs for optimal data review working with users and programmers as appropriate. Implement and execute robust project plans for delivery, ensuring customer needs are addressed in a timely manner. Pro...

Key Responsibilities Programming & Data Handling Write SAS programs to manage, transform, and analyze clinical trial data. SDTM Development Map raw data into SDTM domains following CDISC standards. ADaM Dataset Creation – Develop analysis-ready datasets for statistical analysis and regulatory reporting. TLF Generation – Produce Tables, Listings, and Figures (TLFs) for clinical study reports and FDA/EMA submissions. Validation & QC – Perform independent programming checks to ensure accuracy and compliance. Documentation – Maintain specifications, programming logs, and compliance documents for audits Raw Data Mapping – Extract, clean, and map raw clinical data from multiple sources (EDC, lab, ...

Description Medical Writer II (Clinical Trial Transparency) 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 passionat...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Senior Clinical Data Manager I to join our A-team. The Senior Clinical Data Manager I (SrCDM1) is responsible for leading data management activities of the Allucent Data Management (DM) department. This position manages, coordinates, reviews and approves DM deliverables from database design & set-up, through cleaning and reporting to database locking, ensuring that the completeness, accuracy and consistency of clinical data meets the quality standards and regulat...

You are an experienced Associate Director - Biostatistics who will be joining a leading client in the pharmaceutical industry. Your role will be crucial in clinical development, involving tasks such as contributing to trial design, analysis planning, interpretation of results, and regulatory submissions. Your key responsibilities will include collaborating on innovative and efficient clinical trial designs to ensure alignment with study objectives. You will independently author and review protocols, statistical analysis plans, and clinical study reports. Providing statistical leadership in regulatory interactions, publications, and presentations will also be part of your role. Additionally, ...

Hello Candidates, We are hiring for the Positions of Project Technical Support III for Agra Location. Post Name :- Project Technical Support III Government Project Number of Vacancy : - 04 Age Limit :- 30 yr Essential Qualifications :- Three Years Graduate degree in relevant subject / field + three Years post qualification experience O r PG in relevant subject / field. Monthly Salary :- 28,000/- + 20% HRA = 33,600/- Per month Name of Project: A study to assess silicosis, tuberculosis and their possible risk factors among glass industry, coal-mines and mica-scavengers silica dust exposed workers: An interventional multi-centric study". And A Case Control Study Assessing the Factors Influencin...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Early phase (BABE) statistical data analysis and reporting Statistical protocol inputs and sample size estiamtions Profeciency with regulatory query response and investigations Experience to work with Phoenix WinNonlin & SAS s/w EXPERIEN...

Career Category Research Job Description HOW MIGHT YOU DEFY IMAGINATION If you feel like you re part of something bigger, it s because you are. At Amgen, our shared mission - to serve patients - drives all that we do. It is key to our becoming one of the world s leading biotechnology companies. We are global collaborators who achieve together - researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It s time for a career you can be proud of. Join us. Senior Director Biostatistics What you will do Let s do this. Let s change the world. Amgen is expanding its global Biostatistics capabilities, with A mgen India (A IN ) playing a key role ...

Role & responsibilities Responsible for preparation of PK and Statistical Analysis and Statistical reports (BA/BE and Phase 1) for various regulatory submissions. Provide statistical input and sample size calculations during protocol design Provide statistical/programming inputs for CRF design and review Generate randomization lists Prepare statistical analysis plans Perform blinded statistical review to check for data discrepancies Generate statistical analysis data sets Develop programming requirements documents for SAS programmers Perform data analysis and prepare statistical reports Generate data listings, tables and graphs Develop programs for quality control of analysis programs Provid...

HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission -to serve patients - drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together - researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. Senior Director Biostatistics What You Will Do Let’s do this. Let’s change the world. Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN) playing a key role in integrated delivery and functional leader...

HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission -to serve patients - drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together - researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. Senior Director Biostatistics What you will do Let’s do this. Let’s change the world. Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN) playing a key role in integrated delivery and functional leader...

HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. Senior Director Global Statistical Programming What You Will Do Let’s do this. Let’s change the world. Amgen is expanding its global Statistical Programming capabilities, with Amgen India (AIN) playing a key role in supporting integrat...

We are Hiring for Clinical Research Trainer (Offline) Title: Clinical Research Trainer (Offline) Location: Jayanagar Mode: Offline (On-site) Department: Training & Development Job Purpose To design, deliver, and evaluate high-quality training programs in Clinical Research, ensuring that students/professionals gain practical knowledge and industry-ready skills aligned with current regulatory standards and practices. Key Responsibilities : Deliver offline classroom training sessions on Clinical Research topics such as: Drug Development Process Good Clinical Practice (GCP) & ICH Guidelines Clinical Trial Phases & Protocols Regulatory Requirements (USFDA, EMA, CDSCO, etc.) Pharmacovigilance, Med...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Director - Biostatistics, Lilly Bengaluru At Lilly, we unite caring with discovery to make life better for people around the world. We are a global he...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Associate Director – Statistics, Lilly Bengaluru At Lilly, we unite caring with discovery to make life better for people around the world. We are a gl...

Overview: The Clinton Health Access Initiative, Inc. (CHAI) is a global health organization committed to the mission of saving lives and reducing the burden of disease in low-and middle-income countries. We work at the invitation of governments to support them and the private sector to create and sustain high-quality health systems. CHAI was founded in 2002 in response to the HIV/AIDS epidemic with the goal of dramatically reducing the price of life-saving drugs and increasing access to these medicines in the countries with the highest burden of the disease. Over the following two decades, CHAI has expanded its focus. Today, along with HIV, we work in conjunction with our partners to prevent...

Description Medical Writer II 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 (CTD/CTT) 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, in...

The ideal candidate for this role in Hyderabad should have a minimum of 12 years of experience in the Life Science / Pharma domain, particularly in Clinical development portfolio. This includes expertise in Clinical Data Services from Data Source to Regulatory Submission, covering areas such as Clinical Data Management, Biostatistics, Statistical Programming, and Medical writing. As a key team member, you will be responsible for both new customer acquisition and growing existing customer accounts. Your focus will be on creating a healthy opportunity pipeline to meet business goals related to new Headcount acquisition and Revenue. Developing strong relationships across different buyers in the...

The Clinton Health Access Initiative, Inc. (CHAI) is a global health organization committed to the mission of saving lives and reducing the burden of disease in low-and middle-income countries. We work at the invitation of governments to support them and the private sector to create and sustain high-quality health systems. CHAI was founded in 2002 in response to the HIV/AIDS epidemic with the goal of dramatically reducing the price of life-saving drugs and increasing access to these medicines in the countries with the highest burden of the disease. Over the following two decades, CHAI has expanded its focus. Today, along with HIV, we work in conjunction with our partners to prevent and treat...

Work Schedule Other Environmental Conditions Office At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical ...

every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Biostatistician Technical Expert - Clinical Statistics within our Clinical Statistics Team at Hyderabad, you’ll lead/oversee statistical support of a team of senior and principal biostatisticians, be accountable for statistical aspects and deliverables of the team for several early/late phase studies. Provide directions and guidance in carrying out project assignments, interacting with other internal functions and applying advanced statistical methods while ensuring scientific integrity to projec...

Principal Clinical Programmer (RAVE EDC) Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials. Job Summary Lead in the evaluation, implementation, and validation of packaged systems. Create, maintain, and oversee processes for providing end user support in EDC systems. Build studies and support other users to build studies i...