Biomedical Sciences jobs in Cambridge
- Omnigen Biodata LtdCambridge
- Company pension
- Flexible schedule
- In addition to the above: broad experience of working in life sciences or a medically-related field including general clinical research experience is required.
- SThreeCambridge
- Regulatory Specialists play a vital role in guiding medical device programmes through complex compliance landscapes.
- What roles of this type could offer.
- SThreeCambridge
- Bachelor's degree in Business, life sciences, engineering or a related field.
- We are looking to build our regulatory affairs capabilities through a contract…
- GlaxoSmithKlineStevenage
- Bachelor’s degree in life sciences, biomedical science, or a related discipline.
- The Diagnostic (Dx) Delivery Team within Oncology Translational Medicine is a…
- View all GlaxoSmithKline jobs - Stevenage jobs - Delivery Manager jobs in Stevenage
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- MasimoCambridge CB2 0AW
- The Clinical Specialist is responsible for supporting Masimo Products and maintaining customer relationships with a variety of clinicians and other key…
- View all Masimo jobs - Cambridge jobs
- Salary Search: Clinical Specialist salaries in Cambridge
Deputy News Editor
Often replies in 1 dayAAAS Science International IncCambridge CB2 1LQ- Sick pay
- Life insurance
- Company pension
- Private medical insurance
- Free flu jabs
- Company events
- Strong track record of reporting or editing stories on biomedicine and biomedical policy.
- Fluent writing and deft editing are required, as are strong…
View similar jobs with this employerPA ConsultingMelbourn- A degree in life sciences, pharmacy, engineering, or a related discipline.
- However, the actual time you spend and where you spend it will vary by role or…
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- PA ConsultingMelbourn
- Creating, refining and building a high precision, low noise analogue front end for biomedical instrumentation.
- Shortlisting and/or Technical Assessments.
- RambollCambridge CB1 2JD
- Degree in toxicology, pharmacology, chemistry, biomedical science, biochemistry, biological sciences, food science, veterinary medicine, veterinary science or a…
- View all Ramboll jobs - Cambridge jobs - Toxicologist jobs in Cambridge
- Salary Search: Regulatory Toxicologist- Food & Feed Safety salaries in Cambridge
- See popular questions & answers about Ramboll
- RambollCambridge CB1 2JD
- Degree in toxicology, pharmacology, chemistry, biomedical science, biochemistry, biological sciences, food science, veterinary medicine, veterinary science or a…
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- EnovisLetchworth
- Responsible for the sale of the company’s products within an assigned territory or geographic region.
- Complies with applicable laws in providing physicians with…
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- We are developing all the technologies needed to enable breakthrough AR glasses and VR headsets, including optics and displays, computer vision, audio, graphics…
- LonzaCambridge
- In this role, you will lead client-facing projects involving the design, execution, and optimisation of in vitro cell-based bioassays using human peripheral…
- View all Lonza jobs - Cambridge jobs
- Salary Search: Scientist salaries in Cambridge
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- Many of these programmes start with significant technical uncertainty, where the delivery requirements are still evolving alongside the therapy.
- Alternatively, you may have developed your technical expertise through postgraduate research and discovered a particular aptitude for building relationships,…
- TTPCambridge
- While your background will be in engineering or physics, with core expertise in optical systems, your role will be diverse.
- Life insurance worth 6 x salary.
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Job Post Details
Research Manager
Job details
Full job description
We are currently seeking to appoint a Research Manager to join our growing team at Omnigen Biodata Ltd (“Omnigen”) based in the centre of Cambridge, UK.
Omnigen is a research and development company building the Discover Me Platform—consenting the wider public in the UK and South Africa to build a database and community to support precision medicine studies and trials.
The Research Manager will manage operational activities related to the planning, implementation, and data outputs of Omnigen studies. The activities will be focused on our Discover Me platform.
To learn more about our key platform please visit: www.discovermestudy.org
(note: please do not send job-related queries via the Discover Me study contact details; only applicants contacting us via the Indeed portal will be responded to).
Key responsibilities of the role include:
- develop and execute study-specific plans
- contribute to the development of study protocols
- work with the Head of Research to develop study timelines, including feasibility and recruitment projections
- plan and track site level activities and performance and manage issues relating to execution
- monitor the execution of studies against timelines, deliverables and budget
- conduct QC reviews of essential documents
- maintain oversight of study procurement and logistical aspects of the study (e.g. study equipment)
- maintain the TMF including set up and management of the ISF
- manage vendor selection and associated plans, timelines, budgets and deliverables
- liaise with vendors and suppliers as required
- respond to and track participant queries
- participate in the development of study systems and processes e.g. sample management processes, feedback of results to participants
- lead and participate in study team meetings where relevant
- ensure timelines and deliverables are communicated to all personnel assigned to the study
- ensure appropriate quality measures are in place
- execute inspection readiness activities (TMF review, story board generation)
- contribute to the risk management plans
- supervise direct reports and conduct performance reviews (where relevant)
- participate in process improvement
Qualifications, skills and experience:
The Research Manager will have the minimum qualifications of a bachelor’s degree (BSc, BA or RN equivalent) in a biological or science-related field.
In addition to the above: broad experience of working in life sciences or a medically-related field including general clinical research experience is required.
Preferred requirements:
- demonstrated experience of conducting epidemiological field studies or clinical research studies
- an understanding of the regulatory environment for conducting research studies
- ability to work competently, manage his/her own workload and time efficiently to tight deadlines and to troubleshoot problems without continuous supervision
- detail oriented and highly organised with the ability to ensure accuracy and rigour in all areas of work
- previous management experience of direct reports and the oversight of vendors
- knowledge of ICH GCP and GDPR
Starting salary is dependent on qualifications and relevant experience.
Please submit a copy of your CV with a covering letter summarising your suitability for the role.
Please note only successful candidates will be contacted.
This is a hybrid role with three days in our Cambridge office.
Benefits:
- Hybrid working and flexible hours
- Company pension
Job Types: Full-time, Permanent
Ability to commute/relocate:
- Cambridge, Cambridgeshire: reliably commute or plan to relocate before starting work (required)
Experience:
- conducting clinical or epidemiological research: 3 years (preferred)
Work authorisation:
- United Kingdom (required)
Work Location: Hybrid remote in Cambridge