Lead Biostatistics - Clinical Trials & Submissions
$186.5k - $207kSun Pharmaceuticals, Inc
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 will have a Ph.D. or M.S. in Biostatistics, experience with statistical software, and strong communication skills. The position offers a salary range of $186,500 to $207,000, along with various employee benefits and an annual performance bonus. #J-18808-Ljbffr Sun Pharmaceuticals, Inc
- ...Myers Squibb is seeking an Associate 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...Suggested
- Psi-Cro is looking for a Biostatistics Project Lead in the United States to contribute to statistical activities for global clinical trials. The role involves leading teams, conducting statistical analyses, and collaborating with international project teams. A Master's...Suggested
- Legend Biotech, based in Somerset, NJ, is seeking a Sr. Manager, Biostatistician/Programmer to support clinical trials by providing high-quality analyses and insights from clinical data. This role requires strong programming expertise, particularly in SAS, and a Master’...Suggested
- ...seeking a Sr. Manager, Biostatistician/Programmer to join their Clinical team. This role entails developing high-quality analyses and... ...quantitative discipline and significant experience in clinical trial analysis. This position offers a dynamic work environment with...Suggested
- Bristol Myers Squibb is seeking a Senior Manager, Submission Management Clinical Trials to oversee regulatory activities for clinical trial submissions... ..., preparing submissions for health authorities, and leading continuous improvement initiatives. The ideal candidate...Suggested
- ...biostatistician with a Master's degree in Biostatistics or related field coupled with... ...The successful candidate will lead complex projects, collaborate... ...statistical analysis for clinical research, product development, and regulatory submissions. Strong knowledge of drug...
$72k - $90k
...provider in New York is seeking a Senior Regulatory Consultant to oversee the regulatory compliance of cancer clinical trials. The role involves managing trial submissions, ensuring compliance from approval to closure, and mentoring junior staff. Candidates should have a...- ...pharmaceutical company based in the United States is seeking a Senior Manager, Biostatistics, to provide project support for Real-World Data and Evidence analyses. The ideal candidate will lead statistical studies and collaborate across teams with strong programming...
- A leading cancer treatment center in New York is seeking a Senior Regulatory Compliance Coordinator to oversee clinical trials and ensure compliance with regulatory standards. You will work closely... ...investigators, manage regulatory submissions, and mentor junior staff. A...
- A late clinical-stage rare disease company is seeking a Director/Senior Director of Regulatory Affairs. In this... ..., you will manage global regulatory strategies for submissions in the US, EU, UK, and Japan. You will lead major submissions, engage with regulatory agencies...
- ...Affairs professional to support the implementation of regulatory strategies. Responsibilities include ensuring compliance for product submissions and regulatory interactions. The ideal candidate will have a Bachelor of Science Degree, 5+ years of experience in the...
- Praxis Precision Medicines, Inc. is searching for a Senior Regulatory Submissions Manager to oversee regulatory submissions to U.S. and international agencies. The role requires at least 7 years of experience in the pharmaceutical or biotech industry and strong management...Remote job
- A leading life sciences company is seeking a Regulatory Operations Manager to oversee the publishing of deliverables for electronic submissions to health authorities. The role involves vendor oversight, quality control of submission-related documents, and ensuring compliance...Remote job
- Apr is seeking a Contract Senior Manager, Regulatory Affairs, to oversee the submission of regulatory documents to National Health Authorities. This role requires a minimum of 5 years of regulatory affairs experience in the pharmaceutical or biotechnology sector. The successful...Contract work
$122.25k - $176.58k
## Global Submission LeadBewerbenlocations: Morristown, NJ: Cambridge, MAtime type: Vollzeitposted on: Heute ausgeschriebentime left to apply... ...)job requisition id: R2855370**Job title:** Global Submission Lead* **Location:** Morristown, NJ / Cambridge, MA.**About the job**...WorldwideFlexible hours- Digitas Health is seeking a Senior Associate for Regulatory Promotional Operations to manage complex submission deliverables for pharmaceutical clients. The ideal candidate has a Bachelor's degree and 2-4 years of experience in the industry, along with strong skills in...Work at office
$198k - $289k
...Job Description: Clinical - Standards and Digital... ...generation of clinical trials? Then this function... ...You will drive and co-lead thought leaderships, marketing... ..., ADaM, Regulatory Submission Packages and Data... ...collection standards, biostatistical programming, STDM, ADaM...- ...Neurogene Inc. is seeking a VP of Regulatory Affairs to lead the regulatory strategy and manage submissions like INDs and NDAs. This highly experienced person will work with the Senior VP of Regulatory Affairs to ensure compliance throughout the product's life cycle and...Remote work
- Amgen Inc. (IR) is looking for a dedicated Biostatistics Senior Manager to join its remote team. In this pivotal role, you will lead significant projects, ensuring that all statistical aspects adhere to regulatory standards and contribute to the development of innovative...Remote job
$113 per hour
...client is seeking a Study Lead Statistician (SLS) to... ...for product‑facing clinical studies. The SLS works... ...activities such as regulatory submissions and publications.... ...degree in Statistics, Biostatistics, or a related field... ...reporting of clinical trials within a pharmaceutical...Remote workMonday to Friday$150k - $175k
A leading clinical data services provider is seeking a Senior Biostatistician to offer consulting for statistical analysis in clinical trials. Candidates should have a Master's in Statistics or Biostatistics and 5+ years of industry experience. Proficiency in SAS and a...- Syneos Health is seeking a Principal Statistician Oncology with Submission Experience to lead and mentor biostatistics personnel. You'll be responsible for statistical tasks across clinical trials, collaborating with project teams to ensure high-quality work. The ideal...
- A global clinical research organization is seeking a... ...for oncology clinical trials. The ideal candidate will... ...or MS in Statistics/Biostatistics and at least 8 years of... ...position involves leading the development of statistical... ...to support regulatory submissions. Excellent...
$130k - $160k
A leading diagnostics firm is seeking a Manager, Medical Writing, responsible for overseeing the medical writing team and ensuring high-quality regulatory documents for market submissions. The role includes mentoring writers, managing deadlines, and ensuring compliance...Remote job- A leading healthcare intelligence firm is seeking a Principal Medical Writer to lead the development of regulatory and clinical documents. The ideal candidate will have an advanced degree in life... ..., particularly in regulatory submissions. This role offers a competitive salary...Remote jobFlexible hours
$119.3k - $159.3k
...Regulatory Writer to join its dynamic team in the United States. This role involves developing high-quality clinical and regulatory documents to ensure timely submissions of products. You will also mentor junior writers, ensuring compliance with industry standards. The...- Lead of Medical Writer Location: Beijing-CN Responsibilities Lead the Medical Writing team within Bristol Myers Squibb (BMS) China... ...and scientific documents. Support streamlined, compliant submissions to NMPA and global health authorities, aligning with BMS standards...
$325k - $425k
...Medical Affairs Lead - Osteoarthritis Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient... ...industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...Work at officeLocal areaRelocation3 days per week$60 - $70 per hour
...Job Description Job Description Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality...Hourly payPart timeRemote work3 days per week- Worldwide Clinical Trials Limited is seeking a Site Activation Manager responsible for site activation project management within the Oncology therapeutic area. The role requires overseeing all site activation activities, ensuring milestones are met and compliance with regulations...Worldwide
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Lead Biostatistics - Clinical Trials & Submissions. Be the first to apply!
- clinical research lead New York, NY
- clinical research trainee New York, NY
- clinical research monitor New York, NY
- clinical research manager New York, NY
- clinical research part time New York, NY
- clinical trial associate New York, NY
- clinical trial coordinator New York, NY
- associate director clinical research New York, NY
- clinical trial lead New York, NY
- clinical research New York, NY


