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[Global Role] Clinical Study Lead

Morgan Philips Group SATaipei, Taiwan

30+ days ago

Job description

About the Client

Our client is a global biotech company developing cell-targeting therapies using an unique technology, with the goal to broaden the scope in cancer treatments.

The company provides great talent development opportunities for people who are eager to build a career in a fast-paced environment.

Role's Responsibilities

Leader of 1-3 studies through clinical studies activities that meet ICH / GCP / SOP requirements.
Manage clinical studies from planning to closure including goal-setting, timeline, and budget.
Oversee the performance of study team members in either a matrix management model or as direct reports.
Manage study-related vendors including CROs and contract labs.
Responsible for ensuring development and implementation of applicable study plans, e.g., protocols / amendments, informed consent templates, Communication / Risk Mitigation Plan, eCRF & CRF forms / completion guidelines and site reference manuals / instructions.

Qualifications

7+ years of clinical trial management experience in wither CRO or other biotech / pharmaceutical companies.

Hands-on knowledge and experience in global clinical studies in oncology and managing study timelines, vendor contracts and budgets.

Strong leadership and project management skills and proven ability to multitask.

Excellent communication skills in English.

A team player with the ability to work independently.

Willingness to travel (both locally and globally) depending on the studies activities.

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Global Role Clinical • Taipei, Taiwan