Number of Applicants
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· To develop and write clinical evaluation reports
(CER) for pre - and post -market devices, while ensuring consistency with
regulations, quality standards, commitments and goals.
· Writing coherent, convincing CERs by organizing
and evaluating large amounts of scientific/clinical/medical data.
· Managing CER writing by planning, identifying,
appraising and analyzing clinical data then writing the CER including
conclusions based on expert knowledge.
· Ensuring quality by following internal and
external SOPs, Work Instructions and Forms/Templates for successful preparation
of robust CERs and other documents
· Assisting with other clinical, regulatory,
quality and engineering projects as assigned
· Responsible to acquire, interpret, analyze and
draw conclusions from clinical data from clinical trials, literature and
experiences for a wide variety of medical devices
· Responsible to communicate scientific content in
a clear, concise manner
· Other duties as assigned
· Must be focused, efficient, detail oriented and
able to work independently.
· Able to read, analyze and implement regulations,
standards and guidance.
· Demonstrated ability to manage projects (take minutes,
multi -task, prioritize and ensure reliability and quality while executing
projects on time and on budget).
· Strong written and oral communication skills.
· Bachelor's or Master’s Degree or PhD (preferred)
in a scientific discipline.
· At least 1 -3 years CER writing experience with
solid knowledge of Med Dev 2.7/1, rev 4.
· At least 1 -3 years clinical, regulatory, quality
and/or engineering work experience.
· Able to productively interact with teams
including corporate executives, research sites and research subjects.
· Advanced computer skills with Word, Excel,
PowerPoint, etc.
· Fresh Perspectives
· Enhanced Skills and Expertise
· Increased Productivity
· Improved Morale
· Broadened Network
· Diversity and Inclusion
· Knowledge Transfer
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