Senior Regional Clinical Project Manager (APAC)

Highly Competitive
  1. Permanent
  2. Project/Study Manager (CSM/CPM)
  3. Singapore
Posting date: 14 Aug 2019

An international healthcare leader is advertising a vacancy for a Senior Regional Clinical Project Manager to join their office in Singapore. The company prides itself on its portfolio of life-changing technologies that span the spectrum of healthcare, covering diagnostics, medical devices, nutritionals, and branded generic medicines. With offices in over 160 countries, this is an exciting opportunity to work with a powerhouse in the healthcare field and bolster a career in the field of pharmaceutical marketing.

Job Responsibilities:

  • Manage trials conducted in Asia.
  • Act as a business unit consultant or resource to other business units and external vendor.
  • Provide project management expertise throughout the development and implementation of clinical studies.
  • Interacts with cross function team, vendors/CRO and the business units in order to assist in clinical strategy, the development of study plans, and project deliverables.
  • Provide vendor/CRO oversight and ensure project millstones/timeline are achieved.
  • Lead risk management activities by working with internal & external study team to identify risks to clinical trial implementation and outcomes, present findings to management, and implement basic mitigation.
  • Set quality and compliance goals for the trial and monitor/lead compliance as part of clinical project management.
  • Collaborate with management to develop additional project management tools to improve clinical trial performance.
  • Prepare and update study budget using existing tools.
  • Facilitates communication between CRO, Sales and Marketing, Senior.
  • Identify resource needs for a given trial and elevate any constraints to the management team for resolution.
  • Mentoring junior clinical project manager as instructed.
  • Manage investigational sites by conducting team meetings and by presenting regular updates to management and staff.
  • Monitor spending against specific parts of trial (or trials' program) budget.

Skills and Requirements:

  • Bachelor's degree and 5+ years of related work experience or an equivalent combination of education and work experience. Advanced degree (MS, PhD, MD) preferred.
  • At least 3+ years of clinical trial management, specifically in project management (with cardiovascular or medical device experience)
  • Demand high standards of performance from trial team.
  • Excellent knowledge of ICH-GCP, regulations and policy required for clinical trials in the regional and beyond.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Mandy Fang at or upload your CV on our website -

A full job description is available on request.

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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