medical interpreter jobs in Cambridge, Cambridgeshire

You will collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence. Essential Functions: - Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies.

You will gain practical experience by contributing to two or three projects during the internship, each of which involve the interpretation, assimilation, and creative presentation of clinical or health economic data. Depending on your team and project allocations, you may work on anything from medical communications to market access and evidence synthesis.

About The Job At Alignerr, we partner with the world's leading AI research teams and life-science organizations to build and train cutting-edge AI systems grounded in real-world scientific expertise. Organization : Alignerr Position : Medical Science Liaison (MSL) Type : Hourly Contract Compensation : $35–$75 /hour Location : Remote Commitment : 10–40 hours/week What You'll Do Develop and...

Interaction Engineering Cambridge Job Title: TIG Welder Fabricator We are currently seeking a highly skilled TIG Welder Fabricator to join a leading manufacturer in the medical device and equipment sector. This is a fantastic opportunity to work in a clean, precision-driven environment, producing components critical to healthcare applications. Key Responsibilities: - Perform high-quality TIG...

Senior Quality Engineer Medical Device Startup | £60M Raised Why This Role Matters This is a rare opportunity to join a high-growth medical device startup that has raised £60M from top-tier investors and is scaling rapidly towards global commercialisation. The company is building next-generation medical technologies that will meaningfully improve patient outcomes. As Senior Quality Engineer,...

You will have solid foundations and a flowing book of business to build from. I am looking for an experienced epidemiologist comfortable with leading studies end to end, mentoring and managing a small team of juniors and playing a supporting role in BD/client management.

You will be responsible for identifying, developing, and negotiating new strategic partnerships for Seopa’s comparison solutions portfolio. While insurance comparison is a core focus, experience in other comparison or switching verticals — such as energy, broadband, mobile, current accounts, or credit cards — is advantageous.

You will work closely with product and technology teams to translate regulatory requirements into structured, automated logic that drives an advanced compliance platform. Key Responsibilities • Maintain and expand regulatory intelligence systems across multiple sectors • Translate regulatory requirements into workflows, automation logic, and structured rules

You will contribute to the production of high-quality assessment through work on Multi-Level Testing (MLT) products from test design, materials production, live use, and marking/results.

You will apply your ELT expertise and knowledge of Assessment to the work of MLT, and contribute to the production and delivery of assessments, processes and projects within Assessment and across Cambridge English.

Director- Real World Evidence (RWE) Oncology (Pharmacoepidemiology and Safety) United Kingdom - Cambridge Pharmacovigilance & Epidemiology Regular Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to...

You will collaborate with senior scientists and engineers to support R&D and manufacturing activities.

You will have on‐the‐job learning opportunities to develop expertise in different areas of biobased materials development including formulation, mixing, casting, lamination and finishing.

You will support equally qualified colleagues with a life sciences background, putting to work your prodigious Python skills to advance the state of a growing software platform which forms the bedrock of future research for a global scientific audience.

Job Title Director, Clinical Regulatory Writing Location Cambridge, UK Salary Competitive Introduction to Role Are you ready to lead the charge in transforming breakthrough science into life-altering solutions? As the Director of Clinical Regulatory Writing, you'll be at the forefront of driving strategic communication excellence to achieve successful submissions and approvals. Our team...

You will have primary responsibility for data management (collection of data which involves requesting, tracking, querying, cleaning and reporting) using electronic databases.

You will be required to work with a wide variety of other trials related staff, programmers, statisticians, trial coordinators, monitors, clinicians as well as participating site staff such as nursing and medical.

You will lead customer engagement, coordinate with cross-functional colleagues, and build influential relationships with key NHS stakeholders to ensure patient access to our innovative therapy.

You will also take personal responsibility for leading local projects, analysing territory performance, and sharing valuable insights to inform national strategy.

As an Environmental Specialist III, you will need functional and technical expertise and skills in areas of air, water and/or waste. In this role, you will run projects and programs of moderate complexity that require a specialized breadth of expertise. Your work will challenge you, and with our Core Values to guide you, you’ll quickly learn and grow with us. Responsibilities/Expectations: -...

Senior Business Systems Analyst/Product Owner IQVIA Laboratories IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialise in antibody and...

You will work in project teams alongside experienced colleagues, who provide one-to-one training in the technical aspects of the role, including project management and effective client communication.

You will collaborate with and support expert advisors and event speakers, and the requirement for on-site support at certain events provides opportunities for international travel.

A leading AI and life-science organization is seeking a Medical Science Liaison to develop communication strategies based on clinical trial data and support AI research initiatives. This remote position offers competitive hourly compensation of $35–$75 and a flexible commitment between 10 and 40 hours per week. Ideal candidates will have a background in medical affairs or clinical research and...

You will be asked to provide details of your right to work in the UK within your application, which will be used to help assess your eligibility for visa sponsorship. Please check the following link to read more about the criteria on the UK government website: