Wokingham, Berkshire, South East, United Kingdom Hybrid / WFH Options
Numerus
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 »
Employment Type: Permanent, Part Time, Work From Home
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 »
to support HTA decision-making. Mentor junior colleagues. Contribute to internal training initiatives, process improvement and business development. Requirements University degree in Statistics/Biostatistics or equivalent knowledge/expertise. Knowledge of HTA-related statistical methods, including ITC, NMA, and complex statistical modelling techniques. Awareness of regulatory standards, ICH/ 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 »
Liverpool, Merseyside, North West, United Kingdom Hybrid / WFH Options
ecruit
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 »
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 »
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 non-trial tasks are aligned with the project specifications Responsibitly for continuous development of own skills and to contribute to the development of Biostatistics Providing programming input to the setup of the trial, including but not limited to the CRF, Trial Validation Plan and Data Flow Plan Ensuring that 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 »
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 »
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 »
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 »
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 »
Andover, England, United Kingdom Hybrid / WFH Options
Planet Pharma
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 »
Hertfordshire, England, United Kingdom Hybrid / WFH Options
Planet Pharma
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 »
ophthalmic setting Knowledge and Training Essential Standard keyboard skills Desirable Previous experience using related ophthalmic technology eg Humphrey Visual fields, OCT, Corneal Topography and Biometry Willingness to attend training courses (internal and external) and complete all mandatory training as required by the role Communication & Relationship Skills Essential Good communication skills more »
Winnersh, England, United Kingdom Hybrid / WFH Options
IDEMIA
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 »
the Vice President of Biometrics, you will serve as a key leader within our organization, responsible for overseeing the gloabl Biometrics department, which includes biostatistics, programming, data management, and medical writing teams. You will play a pivotal role in shaping our clinical trial data analysis and reporting strategies, ensuring the … VP, Biometrics is a senior member of the Leadership Team, reporting into the Executive VP. Responsibilities include: Provide strategic leadership and mentorship to the biostatistics, data management, and medical writing teams Develop and maintain a high-performing, collaborative, and results-oriented department Develop core competencies of the group, foster a 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 »
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 »
