Clinical Study Specialist (hybrid)

Proclinical are recruiting for a Clinical Study Specialist to join a pharmaceutical organisation. This role is on a contract basis and is located in London with hybrid working available.

Responsibilities:

• Supervise and update investigator/site status for the trial and assist with clinical trial registry postings.
• Conduct scheduled reconciliations of study trial master file with clinical study lead direction.
• Guarantee scheduled reports are received such as 1572 reportable changes, financial disclosure form, etc.
• Handle and uphold team SharePoint and/or shared drive sites, when required.
• Discuss with sites as directed and uphold site contact information.
• Ather data for assessments, for example: viability and site selection and evaluates site usability database.
• You will track site activation, enrolment and supervising visits to projected plans, and raise any concerns or delays with site activation or deviations from monitoring plans.
• Partake in line listings evaluation for blind data review meetings.
• You might handle or participate in oversight of third-party vendors.
• Contribute to SOPs revisions or divisional initiatives.
• Other duties may be assigned.

Key Skills and Requirements:

• Willing to travel for business needs up to 25% of the time.

If you are having difficulty in applying or if you have any questions, please contact Matthew Pike at m.pike@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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