Salary for clinical scientist

Average salary


4000 £

Basic salary 1900 £
Maximum Wage 6400 £
1900 £
Lowest
4150 £
Average
6400 £
Highest

clinical scientist - How much money do you make working at this position?

The average salary for the clinical scientist position is 4000 £

Companies with the highest earnings in position Clinical scientist
CK INVESTMENT GROUP
Based on 3 job offers
7816 $
7000 £
6400 £
5833 £
5241 £
NORTH WEST PATHOLOGY
Based on 2 job offers
5225 £
5047 £
4480 £
4230 £
GRACE HEALTH AND SOCIAL CARE
Based on 5 job offers
4041 £

Salary in companies


CK INVESTMENT GROUP 7816 $
1900 £ 7816 $
IMC LOCUMS 7000 £
1900 £ 7816 $
WORLD HEALTHCARE 6400 £
1900 £ 7816 $
HOBSON PRIOR 5833 £
1900 £ 7816 $
JAZZ PHARMACEUTICALS UK 5241 £
1900 £ 7816 $
NORTH WEST PATHOLOGY 5225 £
1900 £ 7816 $
REED 5047 £
1900 £ 7816 $
PULSE 4480 £
1900 £ 7816 $
DATAR CANCER GENETICS UK PRIVATE 4230 £
1900 £ 7816 $
GRACE HEALTH AND SOCIAL CARE 4041 £
1900 £ 7816 $

Comment on the job position of clinical scientist

Requirements


  • graduate of an accredited school with B.S. in a healthcare related field.Successful completion of a 1-year internship at an accredited facility.Minimum 3 years' experience as a CLS 1 preferred
  • minimum: Current State of California Clinical Laboratory Scientist licensure
  • recommended: Associated Society of Clinical Pathologists Medical Technologist licensure
  • to provide expert advise on the evaluation and selection of analytical methodology and equipment
  • as clinical lead for clinical biochemistry to assume direct responsibility for maintaining the quality of analytical service to the standards set nationally by United Kingdom Accreditation Service
  • for the monitoring, with the biochemistry service manager, the appropriate use of financial resources and for the management of the principal clinical scientist
  • to have an understanding of the procedures of technologic and method development and evaluation and be able to instruct others in their practical application
  • to be particularly responsible for quality assurance of testing, including external assessment and internal monitoring and taking corrective / preventive action where the need is identified
  • to interpret complex molecular and cytogenetic results requiring a high degree of expertise and specialist knowledge
  • not necessary to have a qualification in medics
  • educated to a PhD, PharmD, or MS degree level would be ideal
  • familiarity with Oncology/Immuno-Oncology
  • comprehension of the drug development procedure from pre-clinical steps through registration and post-registration needed
  • has had in the past, numerous Phase I and Phase II studies as well as a very important Phase III for a collaboration study with an international pharma
  • excellent oral and written communication skills
  • proven ability to work independently and as part of a multidisciplinary team
  • collaborative and flexible in personal interactions with high emotional intelligence
  • willing to travel
  • HCPC registration as a Clinical Scientist
  • first Degree in a biological subject with a strong Genomics component

Responsibility


  • ongoing assignment
  • ASAP start
  • blood Sciences and Biochemistry experience
  • part time opportunities available
  • to be the clinical lead in Biochemistry and to provide a consultant clinical advisory service on diagnosis and treatment of patients to Medical, Nursing staff , GPs and other users of the Trusts Pathology Service
  • for this role, you will assist the newly appointed VP-Clinical Development Leads
  • collaborate with the Medical Directors
  • any other assigned duties
  • assist the senior clinical development personnel on study protocols and amendments cooperating cross-functionally to translate the method and approved concept into implementable, effective clinical protocols and linked documents
  • contribute to or prepare clinical sections of relevant regulatory filings and meeting packages
  • prepare clinical data and clinical program presentations
  • help to identify clinical investigators and coordinate activities for the conduct of clinical trials and advisory board meetings
  • provide input on clinical presentation slides for internal/external meetings and communications
  • provide information, interpretation and comment on national guidance, legislation, codes of practice and answers to Parliamentary Questions and media enquiries
  • to arrange suitable and sufficient cover for reference service delivery, as necessary
  • to be a source of expert advice and information on microbiological aspects of staphylococci and streptococci and the biology of staphylococcal and streptococcal disease
  • provide expert advice and knowledge to external bodies on the scientific basis of reference service tests, documents or services provided as appropriate
  • to present findings of work undertaken at scientific meetings, as appropriate
  • to be responsible for ensuring the high-quality validation of clinical reports issued to customers for staphylococcal and streptococcal reference services, including antibiotic susceptibility testing and molecular detection of resistance mechanisms of public health importance
  • to prepare reports for commercial customers and papers for publication in peer-reviewed journals