Clinical Trials jobs in Buckinghamshire
- PSPAMilton Keynes MK9 3BN
- Annual leave
- An understanding of the pharmaceutical industry and clinical trial processes.
- Facilitate the involvement of patients in research and trials.
- Everest Clinical ResearchUnited Kingdom
- Work from home
- In-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management,…
View similar jobs with this employerImmunocoreAbingdon OX14 4RY- The Translational Medicine Lab plays a pivotal role at Immunocore, generating biological data from both clinical trial and pre-clinical experimental samples in…
- Berkshire Healthcare NHS Foundation TrustReading RG6
- Annual leave
- Employee discount
- Free parking
- Company pension
- Cycle to work scheme
- Car scheme
- E xperience of delivery of clinical research in an NHS setting.
- Having the ability to prioritise and use own initiative to drive clinical research delivery…
- Oxford Health NHS Foundation TrustOxford OX3 7JX
- Annual leave
- Employee discount
- Employee assistance programme
- Company pension
- Car scheme
- Cycle to work scheme
- The post holder will also be responsible for directly managing and supporting patients on early phase dementia clinical trials.
Senior Scientist/Scientist (in vivo)
Often replies in 3 daysBioarchitech LtdOxford OX3 8SB- Sick pay
- Company pension
- Cycle to work scheme
- You will also have the opportunity to oversee contract research organisations (CROs) that conduct in vivo studies of our immunotherapy candidates.
- ImmunocoreOxford OX4 2QF
- Knowledge of the clinical trial/drug development process and/or drug commercialisation.
- Technical and/or scientific knowledge related to biopharmaceutical drug…
- ImmunocoreOxford OX4 2QF
- Knowledge of the clinical trial/drug development process and/or drug commercialisation.
- Technical and/or scientific knowledge related to biopharmaceutical drug…
- Syneos - Clinical and Corporate - ProdUnited Kingdom
- Employee stock purchase plan
- Annual leave
- Sick pay
- Company car
- Performs online clinical literature searches and complies with copyright requirements.
- Completes a variety of documents that may include clinical study…
View similar jobs with this employerUnipharStockley Park- Employee assistance programme
- Work from home
- The Expanded Access Program Manager is responsible for the successful delivery of assigned programs from award through to close-out, ensuring all client…
- NHS ProfessionalsHigh Wycombe HP11 2TT
- Annual leave
- To support training, competency, and accreditation, including intrathecal chemotherapy preparation, clinical trials setup, and mentoring colleagues within the…
- NHS ProfessionalsOxford OX3 7JU
- Employee discount
- Additional leave
- Store discount
- Company pension
- On-site parking
- Transport links
- Provide highly specialised clinical advice to the pharmacy clinical trials team regarding haematology and oncology trials conducted within the Trust.
View similar jobs with this employerLaing O'RourkeOxford- Private medical insurance
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- Laing O'RourkeOxford
- Private medical insurance
- Working closely with the University of Oxford, research partners, consultants, specialist subcontractors and internal delivery teams, you will help create a…
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View similar jobs with this employerUPSLeighton Buzzard LU7 4WG- QP certification of pharmaceutical, clinical trial materials in accordance with IMPDs, PSFs and EU GMPs as well as taking any other QP responsibility as per GMP…
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Job Post Details
Research Coordinator - Maternity Cover (12 months) - job post
Job details
Pay
- £37,127 a year
Job type
- Full-time
Shift and schedule
- Weekend availability
Location
Benefits
Pulled from the full job description
- Annual leave
Full job description
Job Purpose
As the Research Coordinator, you will be responsible for monitoring the progress of our existing research grants, supporting the delivery of PSP and CBD’s first-ever James Lind Alliance Priority Setting Partnership, and scoping the launch of a new grant scheme. You will be reporting to our Chief Executive, James Cusack.
Your priorities will be to:
- Monitor the progress of our research grants.
- Ensure we are funding research which will have the greatest impact on improving the lives of people with PSP or CBD.
- Promote and lead on the involvement of the public and patients in research.
- Help to raise the profile and interest in research into PSP & CBD.
- Maximise the opportunities for people living with a diagnosis to participate in research programmes and trials.
- Maintain our grants management system and ensure our grant management process is in line with good practice in the sector.
- Develop a sector-leading priority setting partnership.
Contract Type
Full Time – Fixed Term Contract (Maternity Leave Cover) for up to 12 months.
Salary
£37,127 per annum full time.
Hours of Work & Annual Leave
- 35 hours per week - this may include working some unsociable hours, including evenings and weekends.
- 28 days plus bank holidays. Pro-rated for part-time role.
The main office is in Milton Keynes, and we have a hybrid working policy with most staff spending one day a week in the office and the remainder working from home. We aim to maximise the time we have together to collaborate and innovate for the benefit of people living with PSP or CBD.
Travel across the UK is necessary.
There is some flexibility for a 4 or 5-day-a-week contract. If you are interested but would like to take the post on less than 5 days a week, please indicate this on your application.
Key Responsibilities
- Work with the CEO and the Chair of the Research Committee to monitor research grants and scope new grant schemes that will continue to drive progress in PSP & CBD research
- Support PSPA’s Research Committee
- Develop relationships with other funders in the neurodegenerative disease field and consider opportunities for co-funding where appropriate to maximise impact
- Develop a sector-leading priority setting partnership.
- Support PSP & CBD research progress wherever possible, including facilitating researcher collaboration, helping with research study participant recruitment and assisting industry with their understanding of patient and carer experiences
- Facilitate the involvement of patients in research and trials.
- Working with the Communications Manager, ensure that PSPA’s research activities and research news are communicated to our community via social, web and print media. This includes writing or contributing to features in PSPA Matters, the charity’s magazine
- Produce lay interpretation for our internal and external audiences relating to complex research matters and outcomes
- Support the Helpline team in responding to calls and emails about research-related topics and in developing research-related literature
- Support the fundraising team in developing campaigns, appeals and applications to trusts for research funding
- Manage PSPA’s research grants portfolio, ensuring adherence to appropriate governance and working with the finance team to track commitment and expenditure, providing detailed reporting to the CEO and Trustees
- Responsible for ensuring the Manual for Managing Research is kept up to date in line with AMRC best practice.
- Develop and maintain relationships with grantees.
- Represent PSPA at research events as well as organise PSPA’s research events including International Symposiums.
The duties may be changed and/or varied to meet changing circumstances at the discretion of the CEO and Board of Trustees.
Person Specification
Essential Criteria:
- A BSc in a biomedical science or strong relevant experience.
- Experience of grants administration and governance, including peer review of applications and reports.
- Commitment to and understanding of the importance of involving the public and people with lived experience in research.
- Some understanding of the neurodegenerative disease research landscape, including potential for collaborations with other funders
- A natural collaborator who will seek to consult on major decisions with the people affected by those decisions
- The ability to work independently with very minimal direction and use initiative to develop ideas for research funding strategy
- Experience of the ability to establish and build relationships with a wide range of audiences including those at a senior level
- Understanding and commitment to equality, diversity and inclusion.
- Strong IT skills and experience with MS Office products
Desirable Criteria:
- An understanding of the pharmaceutical industry and clinical trial processes
- Knowledge of neurological or neuropsychiatric diseases
- A higher degree and some research experience desirable, ideally in neuroscience
For more information about this role, please visit our website.
Corporate Duties
- Ensure you comply with Health and Safety and associated workplace legislation including GDPR, data protection and information security and management requirements.
- Contribute fully to team and staff meetings, promoting the role of the research coordinator within the organisation.
- Promote the vision and goals of PSPA with employees.
- Work within the performance culture at PSPA to consistently achieve your targets and the objectives in your annual appraisal.
- Undertake any other reasonable duties requested of you commensurate with your role and the aims of the charity.