לוח משרות דרושים מחקר במדעי החיים משרה מלאה, לחיפוש זה נמצאו 27 משרות

We have an exciting opportunity for Clinical Research Associate (CRA)!
Summarized Purpose:
Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix.

The Senior Scientist, Antibody Engineering & Discovery, will report to the Head of Antibody Drug Discovery within the Research group. The candidate will participate in antibody discovery, characterization, design, and engineering activities through extensive hands-on laboratory work. The successful candidate will contribute to the generation, engineering, production, and characterization of therapeutic antibodies, including bispecific and multispecific molecules. The role requires strong laboratory skills, scientific rigor, and the ability to independently execute experiments while effectively collaborating with team members.

Responsibilities

Design and generate antibody expression constructs, including antibody engineering activities.
Participate in the production and characterization of recombinant antibodies and proteins.
Perform laboratory-based antibody development activities, including study design, data analysis, and documentation.
Support antibody screening, lead selection, and optimization in therapeutic antibody discovery campaigns.
Collaborate with scientists from multiple disciplines across teams to support project progression.
Present scientific results at team, project, and external scientific meetings, including conferences.
Contribute to the implementation of new technologies and workflows.

we are looking for a Process Development Technician.
Responsibilities:
Prepare media and solutions according to established protocols
Assemble and disassemble bioreactors and related equipment
Clean and maintain bioreactors and supporting tools
Calibrate bioreactors to ensure accurate operation
Perform bioreactor sampling as required
Support the Process Development (PD) team with cell maintenance
Accurately document all procedures and experimental activities
Assist in transferring processes to pilot and production scales

We are looking for a Researcher to join our innovative research team within the Preclinical Department.
In this role, you will contribute to fundamental scientific research focused on understanding biological responses to electric fields at the
molecular and cellular levels.
This is an exciting opportunity for a scientifically driven researcher who enjoys hands-on laboratory work, rigorous experimental design, and translating complex findings into meaningful scientific insights.
You will play a key role in advancing preclinical research while maintaining the highest standards of scientific quality, accuracy, and safety.
What you will do:
Plan, design, and execute experiments in accordance with approved protocols and established scientific standards.
Perform in vitro and in vivo studies to investigate biological responses to electric fields.
Accurately document experimental procedures, observations, and results.
Analyze and interpret data and prepare clear, comprehensive summary reports.
Ensure experimental activities are conducted with meticulous attention to detail and scientific rigor.
Maintain a highly organized working environment and support efficient laboratory operations.
Adhere to all safety requirements and contribute to maintaining the safety of yourself and your colleagues.

We're looking for people who have managed complex technology projects, ideally in healthcare or medical devices. Clinical trial experience and experience working inside pharma partnerships are significant advantages.
Major Duties & Responsibilities
Own end-to-end delivery for assigned programs across pipeline, which may span multiple therapeutic areas, stages of development, and partner-sponsored collaborations.
Manage planning, development, testing, and release of digital protocol features required for clinical and commercial readiness.
Build structured delivery plans covering scope, timelines, risks, and dependencies.
Keep Product, Engineering, QA/RA, Clinical, Medical, Regulatory, CMC, and Therapeutics aligned on requirements, timelines, and deliverables.
Serve as \day-to-day delivery counterpart to pharmaceutical partners: manage joint timelines and deliverables, run partner working groups, and prepare materials for joint steering and governance meetings.
Run cross-team meetings that drive accountability and on-time milestones.
Communicate program status, risks, and mitigation plans to internal leadership and external stakeholders.
Coordinate with external partners, including pharmaceutical partners, CROs, clinical sites, and technology vendors, and manage dependencies where partner decisions affect timelines.
Support preparation of program documentation, training materials, and operational tools.
Ensure delivery processes adhere to QMS and relevant regulatory standards for Software as a Medical Device (SaMD) and clinical studies.