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Job Details

Freelance Clinical Scientist - Pharma - 12 month contract - Berkshire, UK

Company: SRG Clinical
Location: Berkshire, UK
Reference: CSNUK
Closing Date: 25 Aug 17
Type: Contract
Salary (£): Competitive
Benefits: Highly competitive daily rate

Job Summary:

SRG is the market leading supplier of Clinical and Drug development recruitment services to the Life Sciences industries. By putting people at the heart of what we do we are the catalyst that connects the best talent with organisations in the pursuit of ‘Creating Tomorrow’s World’ & helping patients world-wide.

Requirements:

Freelance Clinical Scientist - Pharma - 12 month contract - Berkshire, UK 

Highly competitive daily rate 

protocol writing experience essential 

 

SRG is the market leading supplier of Clinical and Drug development recruitment services to the Life Sciences industries. By putting people at the heart of what we do we are the catalyst that connects the best talent with organisations in the pursuit of ‘Creating Tomorrow’s World’ & helping patients world-wide.

The Clinical Scientist will work collaboratively with the clinical lead and team to execute the clinical program(s). Their primary deliverable is to assist in the assist in planning, executing and reporting of global clinical trials. The clinical scientist support multiple tasks within the categories of: 

 

1) protocol and study design, strategy and training,

2) data review and interpretation, 

3) study scientific integrity and oversight, 

4) safety review and communication, 

5) regulatory document, study report and publication preparation and review.

 

PROTOCOL AND STUDY DESIGN:

  • Support protocol development and protocol amendments
  • Create protocol training materials for site management
  • Provide protocol training at the Investigator meeting
  • Complete clinical sections of the Site Reference Manual
  • Create informed consent form templates, and review site prepared ICFs
  • Support the preparation of other clinical documents as require

DATA REVIEW AND INTEPRETATION

  • Responsible for review of subject level data across a study and for coordinating with the Lead Clinician for study level review as delegated
  • Lead or participate in study analysis and decision point preparation including interim analysis, stopping rules, DMC and DSMB management
  • Interpret data and identify issues of moderate complexity in the data
  • Independently prepares efficient plan for medical review of data

STUDY MEDICAL OVERSIGHT

  • Support the Lead Clinician to provide medical/scientific guidance during the execution of the study
  • Answers specific site management protocol questions as needed
  • Assist in medical issue resolution
  • Responsible for the review of protocol deviation logs

SAFETY

  • Track and reconcile SAEs across a study
  • Report SAEs during Safety Review Team meetings
  • Review and approval of subject narratives as delegated by the Lead Clinician

STUDY REPORT, REGULATORY AND PUBLICATION

  • Participate in development and review of study report
  • Responsible for completion of all narrative writing activities
  • Support study team in developing submissions and addressing reporting and regulatory queries (protocol level).
  • Participate in inspection readiness activities

Qualifications:

  • BA/BS Degree in science or health-related field
  • Advanced education and/or training/experience desirable.
  • Demonstrated ability to support conduct of clinical trials in industry, academic, or research clinic setting
  • Proven scientific writing skills, with strong inter-personal , written/verbal communication skills
  • International clinical trial experience desirable
  • Demonstrated effectiveness in working in a multidisciplinary, matrix team situation
  • Direct therapeutic area expertise may be required in some instances.
  • Understanding of scientific/clinical principles and ability to work across different therapeutic areas
  • must be eligible to work and live in the UK 

How to apply:

Click on the "apply" button today. Alternatively for immediate consideration contact Mariusz Stokowacki at SRG.



Our team at SRG Clinical also cover roles in Clinical Operations (CPM, CRA etc.), Biometrics (Statistics, SAS programming, Data Management), Medical information, Medical Affairs, Pharmacovigilance and Regulatory affairs so do not hesitate to call me us +44 (0)203 964 700.



Key words:
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Apply for this job: Freelance Clinical Scientist - Pharma - 12 month contract - Berkshire, UK

Contact Information:

Address:  Head Office
SRG Clinical 9 Devonshire Square London United Kingdom
EC2M 4HP
England
Tel:  +44 (0)203 096 4700
Website:  Visit Our Web Site

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