Join us in our mission to INVENT the future. Let’s
be part of our team of dedicated, energetic individuals who are committed to be
the most trusted supplier of pharmaceuticals and health products worldwide.
Apply now as Clinical Research Manager to be based in South Korea.
Clinical and Pharmacovigilance teams manage studies to provide the safety and
efficacy data required for regulatory approval of potential new drugs, vaccines
and new indications for existing products. We ensure we conduct high quality
clinical trials by integrating state-of-the-art technology and applying
rigorous scientific and ethical standards.
performance and compliance for assigned protocols in a country in compliance
with ICH/GCP and country regulations, our company policies and procedures,
quality standards and adverse event reporting requirements internally and
drives/tracks execution and performance of deliverables/timelines/results to
meet country commitments for assigned protocols. Strong collaboration with
local loles. Forecasts country resource needs. Serves local business needs
(signs contracts, manages budgets as delegated).
Responsible for quality
and compliance in assigned protocols in country. Oversees CRAs and CTCs.
Oversees training compliance. Performs quality control visits. Reviews
Monitoring Visits Reports and escalates performance issues and training needs
to functional vendor and internal management as needed.
EXTERNAL CUSTOMER FACING
collaboration with functional outsourcing vendors, investigators, other
external partners. Oversees country and site validations, site selection and
recruitment in assigned protocols. Responsible for clinical trial education to
sites. Country POC for programmatically outsourced trials for assigned
with local PV, Regulatory, GMA/GHH to align on key decisions in countries.
Supports local and regional strategy development consistent with long-term
corporate needs in conjunction with CRD and Regional Operations.
Outsourcing vendor, 연구자, 기타 다른 외부
stakeholder들과 협력을 통한
external customer facing 역할
임상업무 약 6-10년 이상 경력자로, monitoring, project manager, people manager,
quality manager 등의 경험이 있는 분
are a research-driven biopharmaceutical company. Our mission is built on the
simple premise that if we “follow the science” and that great medicines can
make a significant impact to our world. And we believe that a research-driven
enterprise dedicated to world-class science can succeed by inventing medicine
and vaccine innovations that make a difference for patients across the globe.
Who we are
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck”
in the United States, Canada & Puerto Rico. We are known as “MSD” in
Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global
biopharmaceutical leader with a diverse portfolio of prescription medicines,
oncology, vaccines and animal health products.
We are driven by our purpose to develop and deliver innovative products
that save and improve lives. With 69,000 employees operating in more than 140
countries, we offer state of the art laboratories, plants and offices that are
designed to Inspire our employees as we learn, develop and grow in our careers.
We are proud of our 125 years of service to humanity and continue to be one of
the world’s biggest investors in Research & Development.
What we look for
In a world of rapid innovation, we seek brave Inventors who want to make
an Impact in all aspects of our business, enabling breakthroughs that will
affect generations to come. We encourage you to bring your disruptive thinking,
collaborative spirit and diverse perspective to our organization. Together we
will continue Inventing For Life, Impacting Lives while Inspiring Your Career
We are proud to be a company that embraces the value of bringing
diverse, talented, and committed people together. The fastest way to
breakthrough innovation is when diverse ideas come together in an inclusive
environment. We encourage our colleagues to respectfully challenge one
another’s thinking and approach problems collectively for the common good. We
are an equal opportunity employer, committed to fostering an inclusive and