Lead Statistical Programmer in Clinical Trials & Regulatory
Creative Solutions Services, LLC
Creative Solutions Services, LLC is looking for a Senior Manager in Statistics based in Hoboken, New Jersey. This role involves overseeing statistical activities across clinical trials, including protocol development and regulatory submissions. The ideal candidate should have a Ph.D. or MS in Statistics/Biostatistics and at least 4-6 years in the Pharmaceutical industry. Strong knowledge of SAS software and industry standards is essential. #J-18808-Ljbffr Creative Solutions Services, LLC
- Lead Programmer Responsibilities Provide technical support and expert advice... .... Lead projects for Statistical programming activities using... ...oversight and guidance on complex trials and submission projects (... ...data listings. Understand regulatory requirements concerning industry...Regulatory
$109.9k - $179.3k
Initial Therapeutics, Inc. is looking for a Principal Statistical Programmer to provide programming support for clinical studies. In this role, you will be responsible for leading programming projects, overseeing data integration, and validating submission requirements...Suggested- ...project delivery, including clinical trial reports and other regulatory submission deliverables. Create statistical analysis outputs to be used... ...to and coordinate and lead a statistical programming team... ...into, and mentor statistical programmers to provide input into...Regulatory
$186.4k - $233k
...Inc. is seeking a Director of Statistical Programming in the United States to lead the Statistical Programming team... ...advancing oncology through innovative clinical trials. Responsibilities include team... ...of programming functions, regulatory submissions, and ensuring data...RegulatoryRemote work- Warman O'Brien is looking for a Senior Statistical Programmer who will lead high-impact statistical programming projects in the clinical trial setting. This role involves close collaboration with clients and regulatory bodies, ensuring data quality while delivering effective...RegulatoryRemote job
- ...the West Coast is seeking a Senior Statistical Programmer to support clinical trial submissions. This role will be... ...ADaM, and TLFs, support ISS/ISE and regulatory submissions (including BIMO), and... ...collaborate closely with statisticians, lead programmers, and external vendors....RegulatoryRemote work
- A leading biopharmaceutical company in New Jersey is seeking a principal statistical programmer to provide programming support for clinical studies. The ideal candidate will possess a Master's degree... ...quality support in the clinical trial process. #J-18808-Ljbffr Regeneron
$186.4k - $233k
This is an exciting opportunity to lead Natera’s Statistical Programming team, specifically focused... ...high-impact, practice-changing clinical trials. As a Director, you will provide strategic... ...clinical trials, programming, and regulatory deliverables. Primary Responsibilities...RegulatoryRemote work$130k - $155k
...biopharmaceutical company leading a new era in the... ...Manager/Senior Manager, Statistical Programming to provide programming... ...role will serve as lead programmer on assigned clinical trials, working closely with Biostatistics... ...submission to global regulatory authorities. As part of...RegulatoryContract workLocal areaRemote work3 days per week- A leading clinical research organization is seeking a Statistical Programming Lead to manage project timelines and coordinate a statistical programming team. The ideal candidate will possess advanced SAS programming skills and strong project management abilities. Candidates...
- ...currently seeking a Senior Statistical Programmer to join us in ROMANIA,... ...expertise for the conduct of clinical trials, acts as an internal subject... ...and complying with regulatory requirements, guidance and... ...strategic vendors. Independently leads and / or performs...RegulatoryRemote workWork from homeWork visaFlexible hours
$110.5k - $122.5k
A leading biotechnology firm is seeking a Manager Statistical Programming to lead statistical programming efforts for clinical studies. The ideal candidate will have over... ...programming clinical trial data with proficiency... ..., contributing to regulatory submissions, and mentoring...Regulatory- ...is seeking a Principal Statistical Programmer to provide programming support for clinical studies in New Jersey.... ...onsite role involves leading programming efforts and... ...in the preparation of regulatory submissions and... ...compliance with clinical trial standards. #J-18808-Ljbffr...Regulatory
$109.9k - $179.3k
...eligible remote. A principal statistical programmer provides timely support to... ...for processing data from clinical studies. Requirements will... ...Support and/or lead programmer for programming... ...and reporting of clinical trials up to regulatory approval, product launch,...RegulatoryShift work- Job Overview Clinical Research Coordinator New York NY 10021 12 months... ...and in compliance with all regulatory, institutional, and... ...Medidata, RedCAP and Clinical Trials Management System (CTMS)) etc... ...queries and/or assist with statistical analyses, as needed. Provides...RegulatoryContract work
- Syneos Health is seeking an experienced statistical programmer with over 8 years in Clinical SAS programming. You will be responsible for developing programming code according to statistical analysis plans, ensuring deliverables meet quality standards, and mentoring junior...
$109.9k - $179.3k
.../Biostatistician to support Clinical Biostatistics within Global... ...feasibility of endpoints and frame statistical approaches to address those... ...pharmaceutical industry and regulatory environment through... ...design and analyze clinical trials. Develop individual protocols...RegulatoryInterim roleInternship$110.5k - $122.5k
Manager Statistical Programming The Manager Statistical... ...expertise to lead and support all... ...support ongoing clinical studies and... ...for study report, regulatory submission, and ad... ...hires and junior programmers. This Role May Be... ...techniques, and clinical trial principles) and...RegulatoryFlexible hours- A Manager Statistical Programming provides timely... ...data from clinical studies. Requirements... ...responsible for leading the programming aspect... ...study through to regulatory approval, product... ...as a lead programmer in the development... ...reporting of clinical trials up to regulatory...RegulatoryPermanent employmentFor contractorsWork experience placementLocal area
- ...Director of Biostatistics to join their dynamic team in Madison, NJ. This role is crucial in designing clinical trials, conducting statistical analyses, and preparing regulatory submissions that affect patients' lives. Qualified candidates should possess a PhD or MS in...Regulatory
- ..., NJ is seeking an Associate Director of Statistical Programming to spearhead statistical programming activities for multiple clinical studies. The ideal candidate will leverage... .... A strong grasp of CDISC standards and regulatory requirements is essential. #J-18808-Ljbffr...Regulatory
- MSD Malaysia is seeking an Executive Director of Statistical Programming located in Pennsylvania, USA. This role involves leading a team to deliver analysis and reporting for clinical trials, while ensuring regulatory compliance and quality. The ideal candidate will have...Regulatory
- A global clinical research organization is seeking a Principal... ...Consultant to provide statistical leadership for oncology clinical trials. The ideal candidate... ...This position involves leading the development of... ...functional teams to support regulatory submissions. Excellent...Regulatory
$200k - $230k
...Director / Director of Biostatistics to lead statistical strategy and execution for clinical development programs. The ideal... ...a strong background in clinical trials. This remote role offers a... ...mentor teams while contributing to regulatory submissions. Travel is limited to...RegulatoryRemote job$128.6k - $210k
Initial Therapeutics, Inc. seeks a Manager Statistical Programming in New Jersey. The role involves providing programming support for clinical studies, leading programming efforts for regulatory approvals, and managing staff contributions. Candidates should have a Master...Regulatory$144.4k - $189.4k
BeiGene, Ltd. seeks a Senior Manager, Statistical Programming Project Lead who will be responsible for leading project development... .... The role entails collaboration with clinical teams and contributing to regulatory submissions. Salary range for this position is...Regulatory- A recruitment agency is seeking a Lead Programmer to provide technical support, lead statistical programming projects using SAS and R, and mentor... ...monitoring, oversight of complex trials, and ensuring compliance with regulatory requirements. The ideal candidate will...Regulatory
- MiniMed is seeking a Senior Clinical Research Monitor to oversee clinical trials while ensuring compliance with protocols and regulatory requirements. This position works closely with clinical investigators and research stakeholders. The ideal candidate should have a Bachelor...RegulatoryRemote job
- Navitas Life Sciences, Inc. is looking for a Senior Statistical Programmer Analyst I to support clinical reporting and programming for regulatory submissions. The role involves SAS programming, analysis, and verification of statistical datasets and deliverables. Applicants...RegulatoryRemote job
$186.5k - $207k
A leading pharmaceutical company in the United States is seeking an experienced Associate Director of Biostatistics. This role involves supporting clinical trials and regulatory submissions, authoring statistical documents, and collaborating cross-functionally. Ideal candidates...Regulatory
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Lead Statistical Programmer in Clinical Trials & Regulatory. Be the first to apply!

