Careers

Thank you for your interest in career opportunities at NeuroDerm.

Here are our current job openings.

We look forward to hearing from you.
Qualified candidates may submit their resume to [email protected]

Global Clinical Trial Manager

Department: Clinical Development

Location: Rehovot, Israel

We are looking for a Global Clinical Trial Manager , to oversee and manage local and/or global trials for all clinical phases, in partnership with other functions.

Job description: 

  • Participate in protocol review, collect and communicate suggestions for a protocol change to responsible author on behalf of Clinical Operations.
  • Collaborate with Supply Chain Management, Medical team, Device Team and RA team to identify vendors.
  • Establish the study budget with assistance from finance and in collaboration with study team.
  • Prepare recruitment projection and select countries and sites with assistance from the CRO and in collaboration with the study team.
  • Review and approve protocol related (ICF/Monitoring/Quality Plans/CRF’s/e-CRF’s) documents and plans.
  • Manage the study team meetings and actively interact with key interfaces such as Medical, Regulatory Affairs, Biometrics, Device etc.
  • Manage the meetings with the CRO at the study level, oversees the CRO and vendors.
  • Ensure all study related manuals are completed, signed and revised as needed.
  • Participate in the review, development and revision of departmental SOPs.
  • Develop in-depth knowledge in relevant indications and clinical trials methodology.

Job Requirements:

  • BSc – a must
  • 5-7 years of Global trials experience
  • Monitoring experience preferred
  • Knowledge of ICH GCP guidelines
  • Fluent English

Formulation Project Leader

Department: Pharmaceutical Development

Location: Rehovot, Israel

We are looking for formulation project leader:

Job Description

Responsibility for preparation and submission of branded drug-device combination in EU and US regulatory agencies:

  • Design and execute pre-formulation, formulation  and preliminary process development
  • Develop novel formulations of poorly soluble drugs in solutions
  • Communicate, write and review SOPs, study protocols and reports to support internal documentation and regulatory submissions
  • Lead formulation development projects and processes independently and as a team player
  • Perform literature search, review and evaluate patent
  • Cross-functional coordination with Analytical, CMC, RA, QA teams

Job requirements:

  • PhD in Chemistry, Chemical engineering, Pharmacy or equivalent
  • At least 10 years relevant industrial pharmaceutical experience in injectable drug formulation development.
  • Exceptional knowledge and expertise with a demonstrated track record in creating strategies to formulate poorly soluble drugs for preclinical and human clinical studies, suitable for regulatory approval
  • Strong written and verbal skills, capable of communicating complex scientific and technical subjects both in English and Hebrew to peer level scientists.
  • Familiar with global drug development requirements, including FDA and EMA
  • Experience with drug-device combination product/s – an advantage

NDA/MAA Submission Lead

Department: RA

Location: Rehovot, Israel

We are looking for an experienced NDA/MAA Submission Lead.

Job Description

Responsibility for preparation and submission of branded drug-device combination in EU and US regulatory agencies:

  • Establish and maintain infrastructure for file preperation and submission
  • Leading the cross functional NDA/MAA project team
  • Manage inovlved consultants and subcontractors, as needed
  • Facilitate interdisciplinary agreement on file submission content
  • Gap analysis to ensure quality submission and compliance with regulatory requirements /commitments to regulatory authorities
  • Overview and integration of submission content
  • Track, interpret and advise on applicable US and European regulations, guidelines, procedures and policies

Job requirements:

  • Global regulatory experience and current knowledge of FDA Guidelines – A must
  • Experience in global pharma
  • Proven Project management capabilities
  • Leadership without authority
  • Excellent interpersonal relations

Experience with drug-device combination product/s – an advantage

System Engineer

Department: Device

Location: Rehovot, Israel

We are looking for an experienced System Engineer for developing new medical device in the drug delivery field (combination product).

Job Description

  • Determine and write product and user requirements for medical device
  • Coordinate technical functions though out the design process for system level behavior
  • Translate requirements into designs that combine hardware, software and mechanics
  • Write test protocols to verify requirements have been met
  • Test sub-systems and system-level software
  • Conduct risk analyses to ensure safe design
  • Provide Input to automated testing tools
  • Document procedures and results within the requirements of a medical device quality management system

Job requirements

Bachelor’s Degree in an engineering discipline And At least 5 years of system engineering experience in medical device industry. Product development lifecycle knowledge is required. Understanding of Medical Device design control.  process. Ability to Work well with other engineers in a collaborative, and to work independently. fast-paced goal-driven environment. High level English and good documentation skills. Proficient in analytical skills, using tools to perform simulations. Willing to travel between local sites and abroad

Software integration Engineer

Department: Device

Location: Rehovot, Israel

We are looking for a Software integration Engineer, to integrate the design and development activities of the SW development team, through the full life cycle of the product, according to the different project stages.

Job description:

  • Have a full and whole understanding of the system and SW design and requirements.
  • Support development cycle of medical device: from user needs, requirements, design, tracking implementation status and release of the products. According to the SW life cycle management, FDA and CE regulation.
  • Support characterization and development of SW tools for R&D testing and production.
  • Hold SW documentation and assist with QA processes.
  • Integrate and collaborate between SW team members, developers, other R&D functions, subcontractors and other key functions.
  • Establish requirements and assessing the suitability (risk, compliance) of current designs and technologies to meet the requirements.
  • Contribute to the assessment of proposed design changes and impact based on test evidence.
  • Provide software support and assistance during usability studies.

Job Requirements:

  • Eng. degree in Biomed, SW or Electronics.
  • At least 2 years of relevant experience in medical device development.
  • Excellent english- verbal and written.
  • Prior experience in SW/system level development of multidisciplinary product.