Strategic Account Executive, Precision Trials - Cambridge, MA

Job Requirements · Company Overview · ConcertAI is building the future of precision medicine. We use advanced artificial intelligence and real-world data to transform how healthcare and life sciences generate evidence, make decisions, and improve patient outcomes—starting in onco ...

· Manage all project team activities related study start up, conduct and close out activities. · Work with Outsourcing and Contracts Management to ensure Site Contracts reflect trial activities and related budget. · ...

· The Opportunity: · As a Senior / Medical Director at Relay Tx, you will help advance our clinical pipeline from IND to proof of concept to registration.  Specifically, you will collaborate with senior medical staff to drive clinical strategy, clinical trial design, and executi ...

· Responsible for the statistical strategy for one or more clinical programs/studies and providing oversight of CRO biometrics deliverablesSupport clinical development team to enable robust study design and execution with a focus on innovative and efficient quantitative decision ...

A clinical-stage biopharmaceutical company developing innovative precision-targeted therapies in oncology requires a Director of Clinical Science ideally an MD with proven track record in early phase oncology clinical development. · Serve as key scientific member of Clinical Deve ...

We are seeking a Clinical Regulatory Specialist to join our team at Iterative Health. · Working alongside research sites on essential regulatory document completion. · Facilitating clinical trial regulatory activity from study start-up through closeout. · ...

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to marke ...

We are seeking a Clinical Regulatory Specialist to join our team. The Clinical Regulatory Specialist will work under the direction of the Chief of Staff with the primary responsibility of assisting research sites with the conduct and compliance of Phase 2-4 pharma-sponsored resea ...

· The Opportunity: · As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH/GCP standards. You will be an integrated member of the Relay ...

We are collaborative and united by a common mission to create transformative genetic medicines for prevalent diseases. · - Plan, drive and oversee all aspects of multi-center global clinical trials in compliance with GCPs, SOPs, and within designated program budgets and timelines ...

· At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively and completely eliminate the root causes of autoimm ...

· The Opportunity: · As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH/GCP standards.  You will be an integrated member of the Relay ...

We are collaborative and united by a common mission. We are building a company with extraordinary people with an audacious vision to create transformative genetic medicines for prevalent diseases. · The Clinical Scientist will work closely with the clinical development department ...

Korro is a biopharmaceutical company focused on developing genetic medicines for rare and prevalent diseases using its proprietary RNA editing platform. · ...

Beam Therapeutics es una empresa biotecnológica comprometida con establecer la plataforma líder para medicinas genéticas precisas. La posición busca un Médico Director para liderar los programas de desarrollo clínico basados en edición genética in vivo. · ...

+Job summary · The Vice President, Compliance is responsible for designing and implementing the company's Corporate Compliance Program to oversee promotional materials and HCP/patient programs.+ResponsibilitiesResponsible for Clinical Supplies Planning and Forecasting as required ...

We are recruiting a full-time academic surgical pathologist with subspecialty expertise in thoracic pathology to join a leading academic medical center. · Strong diagnostic skills · Molecular diagnostics experience (NGS, FISH) · ...

Job Summary</h2Beam is seeking an experienced and motivated Clinical Trial Manager (CTM) to join our growing Clinical Operations team. ...

+As a Senior / Medical Director at Relay Tx, you will help advance our clinical pipeline from IND to proof of concept to registration. · +Collaborate with senior medical staff... · ...

The Sr. Director Clinical Quality Assurance will lead the Quality organization and be responsible for the overall GCP strategy. They will manage audits and inspections, implement quality management systems and lead a high-performing team. · Audit Strategy: Design deliver execute ...