Fetal Medicine Research Assistant

Job title:

Fetal Medicine Research Assistant

Company

NHS

Job description

An opportunity has arisen to join the research team of the Fetal Medicine Research Institute at King’s College Hospital, Denmark Hill, as a research assistance. The Fetal Medicine Research Institute is a major research and clinical unit for fetal diagnosis and therapy. Each year more than 10,000 patients benefit from its services and about 300 doctors, midwives and scientists visit to observe its clinical and research activities. The Fetal Medicine Research Institute has been leading numerous research studies which have been successfully completed leading to more than 1,400 scientific publications in peer-reviewed international journals and more than 50 PhD or MD degrees.Main duties of the jobThe research team at the Fetal Medicine Research Institute at King’s College Hospital has an extensive portfolio covering a range of studies from observational cohort studies to interventional trials for the prediction and prevention of pregnancy complications; and has developed a reputation for excellence in research delivery. An opportunity has arisen for a band 4 research assistant to join the team.The post holder will be part of the team of research fellows and coordinators working to deliver the research studies within the portfolio, in accordance with the principles of Good Clinical Practice. This will include trials with an international profile that are both challenging and interesting. The post holder will manage the database for patients entering the studies but also databases for other research studies in the future. The post holder will ensure clinic appointments/tests required for patients involved in trials are carried out according to the schedule – this will include communicating with research participants via telephone.The successful applicant will have excellent communication skills and a willingness to learn new skills. There is significant patient interaction and a soothing, approachable manner is desirable. For this post you must demonstrate the ability to manage your own workload with supervision from clinical staff; understand clinical trial activity and GCP and be able to complete trial documentation accurately and in a timely manner.About usKing’s College Hospital NHS Foundation Trust is one of the UK’s largest and busiest teaching Trusts with a turnover of c£1 billion, 1.5 million patient contacts a year and more than 15,000 staff based across South East London. The Trust provides a full range of local and specialist services across its five sites. The trust-wide strategy of Strong Roots, Global Reachis our Vision to be BOLD, Brilliant people, Outstanding care, Leaders in Research, Innovation and Education, Diversity, Equality and Inclusion at the heart of everything we do. By being person-centred, digitally-enabled, and focused on sustainability, we aim to take Team King’s to another level.We are at a pivotal point in our history and we require individuals who are ready to join a highly professional team and make a real, lasting difference to our patients and our people.King’s is committed to delivering Sustainable Healthcare for All via our Green Plan. In line with national Greener NHS ambitions, we have set net zero carbon targets of 2040 for our NHS Carbon Footprint and 2045 for our NHS Carbon Footprint Plus. Everyone’s contribution is required in order to meet the goals set out in our Green Plan and we encourage all staff to work responsibly, minimising their contributions to the Trust’s carbon emissions, waste and pollution wherever possible.Date posted04 September 2024Pay schemeAgenda for changeBandBand 4Salary£31,944 to £34,937 a year per annum, inc HCAContractPermanentWorking patternFull-timeReference number213-CORP- 6610220Job locationsHarris Birthright Centre16-20 Windsor WalkLondonSE5 8BBJob descriptionJob responsibilities

• Assist and support research midwives and fellows with accurate completion of trial paperwork. Including; transcribing/exporting data from medical records/GP Surgery/ IT systems to Case Report Forms (CRFs) (paper or electronic) as required by clinical trial protocols, checking eligibility of patients for entry into trials and randomising/registering patients into trials according to protocol requirements.

• Ensure clinic appointments/tests required for patients involved in trials are carried out according to the schedule in the protocol.

• Assist with clinical observations as required by study protocol under the supervision (or direction) of qualified staff and participate in the care of adults requiring a range of clinical interventions, which may include venesection, obtaining blood pressure (electronic), and measuring height and weight (anthropometric measurements). Training will be provided where necessary.

• Responsible for organising a large amount of consent forms arising from the studies, ensuring accurate documentation

Job descriptionJob responsibilities

• Assist and support research midwives and fellows with accurate completion of trial paperwork. Including; transcribing/exporting data from medical records/GP Surgery/ IT systems to Case Report Forms (CRFs) (paper or electronic) as required by clinical trial protocols, checking eligibility of patients for entry into trials and randomising/registering patients into trials according to protocol requirements.

• Ensure clinic appointments/tests required for patients involved in trials are carried out according to the schedule in the protocol.

• Assist with clinical observations as required by study protocol under the supervision (or direction) of qualified staff and participate in the care of adults requiring a range of clinical interventions, which may include venesection, obtaining blood pressure (electronic), and measuring height and weight (anthropometric measurements). Training will be provided where necessary.

• Responsible for organising a large amount of consent forms arising from the studies, ensuring accurate documentation

Person SpecificationEducation and QualificationsEssential

• A’ Level or equivalent Supplemented by a diploma, formal training or equivalent experience.
• Evidence of continuing professional development.
• Degree/ Higher education or equivalent.

Desirable

• Experience of clinical research.
• IT related qualifications 4.
• ICH GCP Trained.

Knowledge and ExperienceEssential

• Experience of data management.
• Administrative experience.
• Evidence of an interest and understanding of a research assistant’s role.

Desirable

• Experience of dealing directly with patients.
• Clinical research experience.
• Previous healthcare environment experience
• ICH GCP training.
• Awareness of current legislation regarding research governance issues.

Skills and CompetenciesEssential

• Proficient IT skills, competent in Excel with advanced keyboard skills.
• Excellent communication skills.
• Good organisational skills.
• Able to prioritise, problem solve and meet deadlines.
• Able to organise own workload.
• Good attention to detail.
• Enthusiastic and able to motivate self and others.
• Ability to work using own initiative, in a flexible atmosphere without close supervision.
• Ability to prioritise work within fast changing environment and meet deadlines.
• Ability to work without supervision and use own initiative Attention to detail.
• Ability to work as part of a team.
• Ability to communicate with wide range of people and demonstrate customer care skills.

Person SpecificationEducation and QualificationsEssential

• A’ Level or equivalent Supplemented by a diploma, formal training or equivalent experience.
• Evidence of continuing professional development.
• Degree/ Higher education or equivalent.

Desirable

• Experience of clinical research.
• IT related qualifications 4.
• ICH GCP Trained.

Knowledge and ExperienceEssential

• Experience of data management.
• Administrative experience.
• Evidence of an interest and understanding of a research assistant’s role.

Desirable

• Experience of dealing directly with patients.
• Clinical research experience.
• Previous healthcare environment experience
• ICH GCP training.
• Awareness of current legislation regarding research governance issues.

Skills and CompetenciesEssential

• Proficient IT skills, competent in Excel with advanced keyboard skills.
• Excellent communication skills.
• Good organisational skills.
• Able to prioritise, problem solve and meet deadlines.
• Able to organise own workload.
• Good attention to detail.
• Enthusiastic and able to motivate self and others.
• Ability to work using own initiative, in a flexible atmosphere without close supervision.
• Ability to prioritise work within fast changing environment and meet deadlines.
• Ability to work without supervision and use own initiative Attention to detail.
• Ability to work as part of a team.
• Ability to communicate with wide range of people and demonstrate customer care skills.

Expected salary

£31944 – 34937 per year

Location

Denmark Hill, South East London

Job date

Fri, 06 Sep 2024 03:34:16 GMT

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