1 to 25 of 29 Permanent Biostatistics Jobs

Career Category Health Economics 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 more »

in a fast-paced environment A 2:1 degree or better in a numerate or science subject, with a relevant PhD degree (e.g. Epidemiology, Biostatistics, Health Data Science) being desirable Excellent grounding in real world evidence with a desire to apply quantitative skills and rigorous science to solving real-world more »

Metric Search is actively representing a Global Contract Research Organisation with the hiring of a Director Biometrics to lead their Biostatistics and Statistical Programming Function across the UK and potentially EMEA. Our client is a CRO that provide full-service support to biotech, pharmaceutical and medical device companies. As the … Director Biometrics, you will lead both the Biostatistics and Statistical Programming teams with oversight, as well as offering key technical input. We are looking for the ideal candidate to have at least 10+ years of industry experience to be considered for these opportunities. This is a perfect position for an … path opening doors to even more senior roles and responsibilities in the not-too-distant future as they continue to grow. Your responsibilities: Lead Biostatistics and Programming Function Lead Statistical support and potential oversight on entire projects, serving as main point of contact with sponsor(s) Be responsible for several more »

working part-time (min 0.8FTE) Play a critical role in making our pipeline accessible to patients. Do you have expertise in, and passion for, Biostatistics? Would you like to apply your skills to impact all phases of drug development and regulatory interactions, in a company that follows the science and … mentor/coach and support the education and training of Statistics staff in the technical arena. Requirements Essential MSc or PhD degree in Statistics, Biostatistics, or related quantitative fields, or equivalent course work/technical experience Understanding of regulations/developments in the area of Clinical Development and Biostatistics Appropriate more »

making our pipeline accessible to patients. We are open to discussing working part-time (min 0.8FTE) Do you have expertise in, and passion for, Biostatistics? Would you like to apply your skills to impact all phases of drug development and regulatory interactions, in a company that follows the science and … mentor/coach and support the education and training of Statistics staff in the technical arena. Requirements Essential MSc or PhD degree in Statistics, Biostatistics, or related quantitative fields, or equivalent course work/technical experience Understanding of regulations/developments in the area of Clinical Development and Biostatistics Appropriate more »

product engineers whilst analysing and interpreting internal product experiments Communicating findings with your team and project partners in a collaborative style Requirements: Ph.D. in biostatistics, statistical genetics, population genetics, genetic epidemiology or MSc with 3+ years' experience in relevant fields. In-depth understanding of genetics, genetic variation, and analytical techniques more »

Mentoring junior colleagues Contributing to internal training initiatives, process improvement and business development Your profile: A passion for statistics University degree in Statistics/Biostatistics or equivalent knowledge/expertise with proven industrial experience Knowledge of HTA-related statistical methods, including ITC, NMA, and complex statistical modelling techniques Awareness of more »

product engineers whilst analysing and interpreting internal product experiments Communicating findings with your team and project partners in a collaborative style Requirements: Ph.D. in biostatistics, statistical genetics, population genetics, genetic epidemiology or MSc with 3+ years' experience in relevant fields. ??In-depth understanding of genetics, genetic variation, and analytical techniques more »

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »

or academic institute; or experience in a closely related discipline within the pharma industry. Or Master’s degree in a field such as epidemiology, biostatistics, statistics, bioinformatics, economics or similar. And significant relevant experience conducting research in the pharma industry, contract research organization, healthcare provider/HTA or academic institute … or experience in a closely related discipline within the pharma industry. Or PhD in a field such as epidemiology, biostatistics, statistics, bioinformatics, economics or similar. And relevant experi-ence conducting research in the pharma industry, contract research organization, healthcare provider/HTA or aca-demic institute; or experience in a more »

Director - Organoid & Tissue Explant Analytics The Director – Organoid and Tissue Explant Analytics will play a key role in the build of the Oncology Translational Research team within GSK Oncology TA . The Director – Organoid and tissue explant analytics will be more »

field. Make a significant impact on developing new treatments. Hybrid working (Liverpool HQ/remote). The Person Bachelor's degree in Life Sciences, Biostatistics, Computer Science or similar. Minimum 3 years' experience in clinical data management, ideally in imaging. Experience with imaging data and software (PACS, DICOM). Knowledge more »

a supervisory role (e.g. line management and/or project management). Minimum requirements as a Principal Statistician: MSc or PhD in Statistics/Biostatistics (or equivalent). At least 6 years of relevant industry experience. Keen to lead a team across a range of projects, ensuring delivery is both more »

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »

working part-time (min 0.8FTE) Play a critical role in making our pipeline accessible to patients. Do you have expertise in, and passion for, Biostatistics? Would you like to apply your skills to impact all phases of drug development and regulatory interactions, in a company that follows the science and more »

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »

and delivery within the Idemia Public Security Business Line for one of our most strategic Travel and Transportation projects in the UK in the biometry and cybersecurity field. The Systems Architect's role is to define and translate our clients' needs into solution/system, act as the coordination point more »

dedicated Clinical Statistical Programmer with a focus on Oncology. This is a remote permanent position. Primary Responsibilities: In this role, you will apply your biostatistics skills and experience to support the development of scientifically based arguments, contributing to fair access to medicines that make a real difference in patients' lives. … You will be part of our Global Biostatistics department, collaborating with multiple functional areas across the company. Skills & Requirements: Advanced degree (MSc or PhD). Proficiency in statistical programming, particularly SAS. Detailed knowledge of CDISC standards (SDTM, ADAM). Excellent communication skills, both written and verbal, with the ability to more »

language. Experience with SAS on PC and UNIX platforms. Qualifications and Experience: • MSc or Ph.D. in Statistics. • 8-10 years of relevant clinical trial biostatistics support in design, analysis, and interpretation. Proven experience of work with clinical trial data in support of safety and efficacy analysis • Ability to read, write more »

Macclesfield, UK Competitive salary and benefits We are open to discussing working part-time (min 0.8FTE) Do you have expertise in, and passion for, Biostatistics? Would you like to apply your skills to impact the early phases of drug development and regulatory interactions, in a company that follows the science more »

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing more »

committee briefing documents). Represent the RWE function in internal cross-functional teams and initiatives. Leverage close collaborations with quantitative functions within CDS (e.g., Biostatistics, Bioinformatics), as well as in Clinical Research, Patient Safety, Medical Affairs, and Global Value and Access to anticipate and meet the evidence needs of regulators … e.g. PhD, MD, ScD, PharmD) and/or Master’s degree (e.g. MSc, MPH) in Epidemiology or related discipline, such as Outcomes Research, Medicine, Biostatistics from an accredited institution, with significant biopharmaceutical industry experience. Direct experience with different applications of RWE, including in support of early-stage clinical development, regulatory more »

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »