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Sub Investigator Clinical TrialsRef: mc 22930

Salary:Up to £60000 per annum

Added:11 Jul 2018

Region: London

Sector: Pharmaceutical

Sub Sector: Clinical Research

An excellent opportunity has arisen to join a leading pharmaceutical company as a Sub Investigator Clinical Trials. JOB SUMMARY The primary responsibility of all investigators participating in the study is for the well-being and interests of their subjects, including subjects enrolled in this study. The Investigator has overall responsibility for the conduct of the trial at his/her study site and may delegate specific duties to appropriately trained members of his/her research team or to other hospital staff, e.g. the pharmacy. Any delegation must be clearly documented in a study site-specific delegation list. The Investigator is responsible for the following: JOB DUTIES: Role Specific: 1.Working under the direct supervision of the Principal Investigator 2.Performing the study in accordance with ICH GCP 3.Ensuring that adequate time and appropriate resources are available to perform the study as described in this protocol 4.Ensuring that all persons assisting with the trial are adequately qualified persons to whom duties have been delegated 5.Signing an Investigator Agreement to confirm acceptance and willingness to comply with the study protocol 6.Maintaining adequate records of each subject's participation 7.Managing the clinical trial team - supervising, mentoring, training, risk management etc. 8.To undertake specific administrative duties as required including appropriate record-keeping 9.To perform other duties of a similar nature appropriate to your position which may be required from time to time by the line manager 10.Plan and prioritise own workload 11.Work within Company operational and professional guidelines General company responsibilities: 1.Take personal responsibility for accessing, understanding and learning the Company's policies and procedures that are relevant to the role and that are generally applicable to working within the organisation 2.To be responsible at all times for one's own health and safety in line with the Organisation's Health and Safety policy and procedures and that of others in the organisation, including patients and visitors 3.Act at all times in a responsible and professional manner, projecting a high quality and high service experience to all stakeholders and patients 4.Work to high ethical standards in line with Company policies and procedures 5.Work collaboratively with colleagues to deliver services effectively and efficiently 6.To be of smart appearance and exhibit appropriate behaviour with colleagues and patients 7.To ensure the Company's objectives and values are embedded in everyday routine 8.To ensure that all data and records are safely handled with regard to privacy and confidentiality, including physical patient's files and data on systems and ensuring adherence to the Data Protection Act 1998 9.To perform any other duties that are reasonably requested by the organisation from time to time Key People is a specialist international recruitment consultancy with over 25 years' experience of working within the life sciences, biotech, healthcare and CRO industries. Our experienced and dedicated clinical research related consultants have a long history of success, excellent technical knowledge and a flexible, consultative focussed approach to recruitment. Please contact Mark Cussens, Clinical Research Recruiter on Tel: +44 1727 817623 or email: mcussens@keypeople.co.uk Tel: +41 4350 86620 or email: mark.cussens@keypeopleswitzerland.ch Key People is a recruitment company with a reputation fpr providing good value that's been built up over 20 years. -We achieve results faster -Our candidates really are a cut above -We add greater value We think it's because we're a private company driven by clients, not by shareholders. For our candidates, we have developed relationships with thousands of clients nationwide and across Europe, who choose to recruit through Key People, so you'll have a wide choice of opportunities to further your career.

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