Lead Statistical Programmer in Clinical Trials & Regulatory
Creative Solutions Services, LLC
Job Description The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing. Responsibilities Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc. Review CRF, database design, and edit check specs. Review study quality surveillance plan and monitor study conduct. Prepare and/or review SAP, TFL shells and specifications for variable derivation. Work closely with Statistical Programmers and Clinical Data Manager to identify data quality issues for key efficacy and safety variables. Provide statistical and validation support for statistical analysis, analysis datasets and TFL. Review study report, manuscripts and other documents related to statistics. Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents. Perform other ad-hoc statistical activities as needed. Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming. Participates in monitoring CRO activities and reviewing CRO deliverables. Other duties as assigned. Requirements Ph.D. or MS in Statistics or Biostatistics. Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience. Excellent knowledge of SAS computer package. Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines. Excellent organizational skills, time management, and ability to meet established deadlines. Excellent communication and interpersonal skills to effectively interface with others. Ability to work independently and problem-solve. Ability to provide leadership for the CRO statisticians and statistical programmers. #J-18808-Ljbffr Creative Solutions Services, LLC
- ...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....Regulatory
$200.09k - $217.9k
...company is seeking an Associate Director, Statistical Programming to lead programming activities for studies.... ...analysis, dataset maintenance, and regulatory compliance in a hybrid work model.... ...in statistical programming and clinical development. The base salary range is...Regulatory- ...Protocol, CRF, and SAP. Create and assess statistical programs in SAS and/or R to produce... ...involvement as a production or QC programmer at both product and study levels. Strong... .... In-depth understanding of FDA regulatory guidance around Study Data and Submission...Regulatory
$200.09k - $217.9k
Associate Director, Statistical Programming page is loaded## Associate... ...for data integration used for clinical summaries and/or creation and... ...submission components to regulatory agencies. May partner with biostatisticians... ...for multiple studies and lead the programming submission...Regulatory$175k - $185k
...along the way, come join the Broadridge team. We are seeking a Lead Security Engineer to join our global Security Engineering Team.... ...resilient security infrastructure aligned with business and regulatory requirements. Oversee onboarding of critical applications to...RegulatoryLocal areaWeekend work- ...Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position... ...Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as...Regulatory
- ...Statistical Programmer Candidate to develop standard global data review tools... ...and figures for oncology trials. Ensure timelines and... ...Master Analysis Plan, GCP and Regulatory Guidelines). Comply with... ...preferred. Knowledge about clinical trials a plus. Ability to...RegulatoryWork experience placement
$160 - $180 per hour
...Monitor tasks include: Provide clinical development support... ...clinical management, biometrics, regulatory, pharmacovigilance, and CRO... ...and reporting of clinical trials and related regulatory deliverables... ...consent documents Statistical analysis plans (in collaboration...RegulatoryHourly payContract workFor contractorsRemote work$273.2k - $358.6k
...Executive Director, Clinical Data Science At Eisai... ...rigorous application of statistical principles and... ...to optimize clinical trial efficiency and accelerate... ...representative to global regulatory authorities, this individual... ...Authority meetings, leading preparation of...Regulatory- ...CROs, and Sites across the research and clinical trials landscape. By blending deep subject... ...coordination. A central focus of the role will be leading the operational build‑out and execution... ...‑up optimization, IRB processes, and regulatory compliance. Experience with CTMS...RegulatoryFull timeTemporary workFlexible hours2 days per week3 days per week
- ...leadership to develop Clinical Development Plan (CDP)... ...partners in Pre-Clinical, Regulatory, Safety, Stats, &... ...Plans (CDPs), clinical trials and protocols and execute... ...GCP) regulations ~ .Lead high quality planning... ...trial design, statistics, and regulatory and clinical...RegulatoryFlexible hours
$160k - $241k
Tango Therapeutics is seeking a Clinical Trial Leader (CTL) to execute clinical trials in a fast... ...-paced biotech environment. You will lead cross-functional teams, managing the... ...setup and conduct of trials while ensuring regulatory compliance. This role requires strong...Regulatory$215k - $295k
...in Florham Park, NJ. This role focuses on developing COA strategies for patient-centered clinical trials, providing leadership to cross-functional teams, and ensuring regulatory acceptability of endpoints. The ideal candidate will possess a Master's or PhD and at least...Regulatory- Rutgers University is seeking a Clinical Research Associate in Newark, NJ. This individual will be part of a multidisciplinary team, focusing on regulatory compliance and coordination of research protocols in accordance with institutional guidelines. Qualifications include...Regulatory
$198k - $289k
...Job Description: Clinical - Standards and Digital... ...generation of clinical trials? Then this function... ...offers in the clinical, regulatory and safety domain.... ...You will drive and co-lead thought leaderships, marketing... ..., pharmacist, statistics) or equivalent by expertise...Regulatory- Merck & Co. is seeking a Clinical Quality Operations Manager in Rahway, New Jersey to lead the quality management in clinical trials. The role involves developing quality strategies,... ...and ensuring ongoing compliance with regulatory standards. The ideal candidate will have...Regulatory
$222.4k - $278k
...and executing translational, clinical pharmacology and... ...of MIDD using population and statistically based methodologies, as well... ...to Make a Difference Lead clinical pharmacology and pharmacometrics... ...functional lead for global regulatory activities and HA...Regulatory- ...miles west of New York City. Job Description Responsible for leading the design, development, and implementation of manufacturing processes... ...downtime, scrap). Ensure compliance with safety, quality, and regulatory standards. Develop budgets and capital expenditure plans for...Regulatory
- ...CORE JOB RESPONSIBILITIES: Assist the Clinical Research team to interface with... ...Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management. Review and... ...interpersonal skills. Knowledge of clinical trial design, basic statistics, and data...RegulatoryPermanent employmentContract workWork at officeImmediate start
- Pinnacle Clinical Research in Springfield, NJ is seeking a Quality Associate to ensure the quality of clinical trials. Responsibilities include performing audits, ensuring compliance with regulations, and training site staff. Candidates should have a Bachelor's Degree...Regulatory
- ...Summary (On-site) The Clinical Development Executive... ...strategy in line with regulatory requirements and sound... ...data from clinical trials and other permitted sources... ...team, the role leads medical strategy and supports... .... Must be facile with statistical issues and be able to...RegulatoryContract work
- ...Axiom SL Technical Lead Integrated Resources, Inc is a premier staffing firm recognized... ...areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and... ...Strong Axiom Controller Deep knowledge of Regulatory Reporting for US and Foreign Bank...Regulatory
- ...Manager, Statistical Programming - REMOTE Join to apply for the... ...a team of Statistical Programmers in the research and development... ...role is responsible for leading statistical programming... ..., Medical Writing, Regulatory Publishing, and Clinical Operations. Responsibilities...RegulatoryFull timeRemote work
$45 - $60 per hour
...a pivotal role in the execution and management of oncology clinical trials. This role blends clinical expertise with research precision... ...are conducted safely, ethically, and in full compliance with regulatory standards. This position is essential in advancing cancer care...RegulatoryHourly payImmediate startFlexible hoursShift work$87k - $113k
.... Selective's unique position as both a leading insurance group and an employer of choice... ...in compliance with applicable legal and regulatory requirements. Note: (For NJ... ...Degree in Mathematics, Actuarial Science, Statistics or Economics preferred. ~2 years of Property...RegulatoryWork experience placementInterim role- ...This is a contractor RTH role . This individual will lead the technology strategy and projects related to the client's new direct... ...solutions to drive business and revenue growth, ensure trading regulatory compliance and implement efficiencies. Extensive contact with...RegulatoryFor contractorsFlexible hours3 days per week
$55.55 - $68.75 per hour
...Nuclear Med Tech Lead Req #: 0000244791 Category: Radiology / Imaging... ...established by the hospital, state and federal regulatory agencies Performs all duties in a... ...education, and research to address both the clinical and social determinants of health....RegulatoryHourly payFull timeTemporary workWork experience placementLocal areaRelocation packageFlexible hoursShift workDay shift- ...schedules to ensure Workforce Management system is able to provide statistical staffing requirements based upon current staffing... ...be used in determining compensation. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances...RegulatoryRemote jobHourly payMinimum wageFull timeContract workTemporary workWork experience placementImmediate startHome officeShift work
$119.7k - $222.3k
...the role: The Statistical Programming community... ...) statistical programmers and belongs to the... ...portfolio of clinical projects across the... ...within the clinical trial/program, ensuring... ...: * Lead statistical programming... ...reports (CSRs), regulatory submissions/interactions...RegulatoryWork experience placementRemote work- ...RRT Hospital Supervisor—lead Respiratory Care on a nights position in Northern New... ...teach and precept; active research with clinical trials and IRB support; clinician-led innovation... ..., favorable access to regional tax and regulatory advantages, an engaged civic climate,...RegulatoryFlexible hoursShift workNight shift
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