Clinical Study, Associate Manager (Hybrid)

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

Responsibilities:

• Supervise progress for site activation and oversight visits.
• Monitor the implementation of the specific Clinical Study deliverables against planned timelines.
• Raise any concerns linked to timelines or budget to Clinical Study lead.
• Assist on data quality which involves routine evaluation of data metrics and listings, protocol deviations, eligibility violations, dosing deviations and suspected non-compliance by sites.
• Raise data flow and data quality concerns to Clinical Study lead.
• Partake in the development of and supervise execution of recruitment and retention methods.
• Evaluate site level notified consents and any other patient-facing study start-up resources.
• Offer routine status reports to shareholders as requested by the Clinical Study lead.
• Other duties may be assigned.

Key Skills and Requirements:

• Educated to a degree level with relevant work experience.

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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