Position Description

Clinical Research Associate/Lead, Medical devices/Pharma (Immediate, EDC, Up to $5K)
Job Code 18575
Job Placement Location Singapore
Apply Now
  • Our Client is a well-established Medical industry, has presence in Asia with a direct offices within the Region.


  • To implement and oversee projects, and ensure quality of trials.
  • The CRA outline project together with client and clinical monitoring team.
  • To regularly visits Clinical Trial Investigators, issues them supplies, such as Case Report Forms and Investigational Product.
  • Gather Case Report Forms and ascertain their quality, and collaborate with Clinical Trial Investigators to write final technical reports.
  • To ensure the project meets the client's goals within budget and on time.

Key Responsibilities:

  • Set targets for clinical monitoring staff and ensuring recording of trial in compliance with project goals.
  • Creating and implementing study-specific clinical monitoring tools and documents.
  • Creating and overseeing trial budget.
  • Coordinating and supervising clinical monitoring team.
  • Providing Clinical Research Associates with project-specific training and having regular meetings with them.
  • Recording and sharing interactions with client and acting as their representative.
  • Arranging and overseeing site visits.
  • Gathering and examining trial documents.
  • Assuring compliance SOPs and local regulations, and CFR, ICH and GCP guidelines.
  • Provide leadership role to overseas CRA (where applicable).


  • Bachelor’s Degree in Nursing or Life Sciences.
  • Minimum 4 to 5 years' relevant working experience in Clinical Research, from Medical devices or Pharmaceuticals industry.
  • Proficient in MS Office applications, especially MS Excel.
  • A multitaskers and client-oriented, willing to be hands-on.
  • Independent and have the ability to prioritize tasks.
  • Proficient understanding of SOPs related to clinical trials.
  • Outstanding communication skills, both verbal and written; she/he will work closely with Taiwan, Thailand, Korea counterparts.
  • Understanding of Electronic Data Capture (EDC).
  • Ability to travel Islandwide (few times in a month), Overseas as and when required.

Other Information:

  • Reporting to CEO and Principle Investigator (of the Clinical trial - based in Hospital).
  • Working Location: Central. 
  • Working Hours: Mondays to Fridays, 8am to 5pm.
  • Critical: Due to the organization's affirmed support and commitment to developing a Singaporean core, this role is only available to Singaporeans.

To apply, please visit www.gmprecruit.com and search for Job Reference: 18575.
To learn more about this opportunity, please contact Novita Tan at novita.tan@gmprecruit.com
We regret that only shortlisted candidates will be notified.
GMP Recruitment Services (S) Pte Ltd | EA License: 09C3051 | EA Personnel: Novita Tan | Registration No: R1220374

Back Apply Now