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Job DescriptionAre you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, r...

Job Description Dyania Health is a venture-backed company founded in 2019 which has developed Synapsis AI, an end-to-end system that combines a medically pre-adapted and fine-tuned large language model (LLM) with a physician-driven algorithmic reasoning engine to understand and assess clinical ch...

Job Description About Tonix* Tonix is a biopharmaceutical company, publicly traded on NASDAQ (ticker: TNXP). The Company is focused on commercializing, developing, discovering and licensing therapeutics to treat and prevent human disease. Tonix markets Zembrace® SymTouch® (sumatriptan injection)...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job DescriptionJob description Job description Job Overview Board Certified Behavior Analyst (BCBA) Applied ABA Therapy is a premier provider of Applied Behavior Analysis (ABA) services, committed to transforming the lives of individuals with autism spectrum disorder (ASD) and other development...

Job Description Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, ...

Job Description WHY VITALIEF? Vitalief is a trusted partner working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job Description About Tonix* Tonix is a biopharmaceutical company, publicly traded on NASDAQ (ticker: TNXP). The Company is focused on commercializing, developing, discovering and licensing therapeutics to treat and prevent human disease. Tonix markets Zembrace® SymTouch® (sumatriptan injection)...

Job Description About MMS Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified org...

Job Description Overview: Vitalief is a trusted partner working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Fun...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job Description Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, ...

Job Description Job Title: Registered Dental Assistant Department: Operations Reports to: Dental Practice Manager FLSA Status: Non-Exempt Company Overview ProSmile is one of the fastest-growing dental organizations, with a vast network of multi-specialty practices across New Jersey, Pennsylvani...

OnLibra connects pharmaceutical and biomedical research teams with highly specialized information science talent. Whether you’re navigating a complex regulatory submission, building a controlled vocabulary system, or scaling your knowledge infrastructure, we deliver experts who get the job done....

Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets. The Clinica...

Job Description The Biologics Analytical Research & Development department of our company Research Laboratories Division is seeking applicants for a Principal Scientist position available at its Kenilworth New Jersey research facility. The Principal Scientist is a senior scientific role taske...

Job Description: • Working with the Biometrics staff the candidate will provide programming support for Phase 1 to Phase 3 studies. Providing timely support to the project team on all statistical programming matters according to the project strategy., • The candidate programs SDTM/ADaM/TLFs fo...

Band Level 5 Job Description Summary We are looking for a leader of our 20 Clinical Data Acquisition Specialists Clinical Data Scientists and Coding Specialists. This key role will ensure adequate staffing/resource allocation for the delivery of the portfolio to the TA area (managing attrit...

Job Description Summary We are looking for a leader of our 20 Clinical Data Acquisition Specialists Clinical Data Scientists and Coding Specialists. This key role will ensure adequate staffing/resource allocation for the delivery of the portfolio to the TA area (managing attrition hiring talent ...

Serves as Clinical Trial Lead for one or more trials + Successfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervision + Provides scientific and clinical leadership to team of supporting Clinical Scientists (matrix leadership)

Position Summary** • Serves as a primary source of medical accountability and oversight for multiple clinical trials • Matrix management responsibilities across the internal and external network • Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities

Clinical Development, Clinical Trial Planning, Dermatology, Dermatology Research, Launch Strategy, Market Access, Medical Affairs, Medical Dermatology, Medical Research, Pharmaceutical Medical Affairs, Pipeline Strategy, Project Management, Scientific Engagement, Strategic Thinking. Global Direct...

Ensure lessons learned are communicated across teams and ensure alignment so that unnecessary amendments are avoided and to align with asset/TA-level protocol elements + May serve as Trial Lead for complex clinical studies + May present data/information to internal and external stakeholders

Associate Director, Regulatory Affairs. We are seeking an experienced Senior Manager to Associate Director, Regulatory Affairs, to manage our regulatory clinical trial applications (CTAs) and compliance efforts. In this role, they will excel in developing and executing global CTA submission strat...

Clinical Data Management Leadership.Provide clinical data management leadership within the study team to align on and drive data collection requirements for one or more complex clinical development projects.Efficiently plan, coordinate, and deliver complete, high quality and reliable clinical tri...

Position Summary / Objective** + Serves as a primary source of medical accountability and oversight for multiple clinical trials + Matrix management responsibilities across the internal and external network + Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabili

Actively participates in internal Trial Supply Management and Clinical Supply Chain meetings, Study Team meetings, Clinical Supply Matrix Team meetings and any other relevant meetings providing all relevant data and documentation prior to each meeting, highlighting any risks and mitigation strate...

This position provides legal oversight for the negotiation and management of clinical trial agreements, grant-funded research contracts, and collaboration agreements with academic and industry partners. Demonstrated ability to manage complex agreements and collaborate effectively with operational...

Primary Responsibilities:** + Chair the Clinical Supply Program Team and works closely with Clinical Trial Teams (CTT), Project Management (PM), Regulatory, and other functional area representatives to negotiate timelines and strategy for clinical supplies + Acts as the main spokesperson between ...

Responsibilities: We are seeking a skilled Clinical Data Management Lead to oversee the execution of clinical trials.This role will be responsible for ensuring high-quality data collection, review, and delivery within scope, on time, and with precision.Lead clinical trial project teams, attending...

Responsibilities include : * An academically oriented, COC accredited multidisciplinary cancer program with the following components * Extensive clinical trial menu from phase IB through phase III * Multidisciplinary conferences covering all areas of hematology and oncology * On-site infusion ser...

May be assigned to lead clinical trial(s) as Clinical Scientific Lead and provide leadership and guidance for all clinical aspects of a clinical trial. As the medical/clinical lead interacts with and represents Novartis to global key opinion leaders and experts and may lead or co-chair steering c...

As a Head of Product at EVYD Technology US, you will lead the strategy, development, and execution of our next-generation AI-powered clinical trial optimization platform. This is a high-impact leadership role where you will shape the future of AI in clinical development, working closely with AI e...

The Global Executive Director, Development Real-World Evidence is part of the Clinical Development group and provides strategic oversight and direction for development RWE generation with a focus on supporting clinical trial designs and observational studies to generate innovative and new treatme...

Safety Reports) + Ensure collation and distribution of study tools and documents + Update clinical trial databases (CTMS) and trackers + Clinical supply & non-clinical supply management, in collaboration with other country roles + Manage Labeling requirements and coordinate/sign tran

Are you eager to earn extra income from the comfort of your home? We are looking for motivated individuals to participate in paid research studies including focus groups, clinical trials, online surveys, secret shopping, and product reviews. Join Our Part-Time Research Studies Today!. This is an ...

Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 25% Flexible Work Arrangements: Remote Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Required Skills: Clinical Development, Clinical Trial Planning, Dermatology, Dermatology Re...

The Senior/Clinical Development Director (Sr*CDD) is the clinical/scientific expert and if assigned the clinical development lead of a section of a global clinical program and/or trial. Clinical deliverables may include the clinical development strategy for assigned program section(s), clinical s...

Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data.Develop and maintain department/system-level macros.Create and review SDTM and ADaM specifications.Create and validate SDTM data sets.Create and validate analysis data sets.Create and validate patient prof...

As a Clinical Development Medical Director in Cardiovascular Renal & Metabolic, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. Need thorough knowledge of Good Clinical Practice, clinical trial des...

Provides expert safety input to the clinical development program for assigned projects/products and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) -Is responsible for safety issue management from formation of Global Program Team (GPT...

The Vice President/Head of Global Clinical Operations is a senior leadership role responsible for overseeing all aspects of clinical trial execution within a pharmaceutical or biotechnology company. The base salary range for the Vice President, Global Clinical Operations is from :347,400-456,000U...

Join Our Part-Time Research Studies Today!. Are you eager to earn extra income from the comfort of your home? We are looking for motivated individuals to participate in paid research studies including focus groups, clinical trials, online surveys, secret shopping, and product reviews. This is an ...

Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas. About the role:...

Job Description About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a ...

As a Clinical Development Medical Director, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. Support the Clinical Development Head by providing medical input into CDP and clinical trial package revi...