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Taiwan Biotech Jobs (NOW HIRING)

Everest Clinical Research

Proposals Manager (Remote)

$95K - $130K/yr

... biotechnology, and medical device industries. We serve some of the best-known companies and work ... Taipei, Taiwan; and multiple offices in Europe. Everest is known in the industry for its high ...

rinchem

Warehouse Technician

Bensalem, PA

$16.25 - $20/hr

... biotech, pharmaceutical, aerospace and defense, and other manufacturing industries to streamline ... Rinchem has active operations in the United States, Israel, South Korea, Taiwan, Ireland, and ...

rinchem

Warehouse Technician

Bensalem, PA

$16.25 - $20/hr

... biotech, pharmaceutical, aerospace and defense, and other manufacturing industries to streamline ... Rinchem has active operations in the United States, Israel, South Korea, Taiwan, Ireland, and ...

Rinchem Company, Inc.

Warehouse Technician

Decatur, GA · On-site

$16.50 - $20.50/hr

... biotech, pharmaceutical, aerospace and defense, and other manufacturing industries to streamline ... Rinchem has active operations in the United States, Israel, South Korea, Taiwan, Ireland, and ...

rinchem

Final Mile Driver

Surprise, AZ · On-site

... biotech, pharmaceutical, aerospace and defense, and other manufacturing industries to streamline ... Rinchem has active operations in the United States, Israel, South Korea, Taiwan, Ireland, and ...

Everest Clinical Research

Senior Biostatistician

$130K/yr

... biotechnology, and medical device industries. We serve some of the best-known companies and work ... Taiwan. Everest is known in the industry for its high quality deliverables, superior customer ...

Rinchem Company, Inc.

Warehouse Technician

Bensalem, PA · On-site

$16.25 - $20/hr

... biotech, pharmaceutical, aerospace and defense, and other manufacturing industries to streamline ... Rinchem has active operations in the United States, Israel, South Korea, Taiwan, Ireland, and ...

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Taiwan Biotech information

What are some typical challenges faced by professionals working in Taiwan's biotech industry, and how can they be addressed?

Professionals in Taiwan's biotech sector often encounter challenges such as navigating complex regulatory requirements, keeping pace with rapid technological advancements, and working in multidisciplinary teams. Overcoming these hurdles usually involves continuous professional development, proactive communication with regulatory bodies, and strong collaboration with colleagues from diverse backgrounds, such as research, manufacturing, and business development. Being adaptable and open to learning new skills is key to thriving in this dynamic environment.

What is a career in Taiwan biotech?

A career in Taiwan biotech involves working in the biotechnology industry in Taiwan, which includes pharmaceutical development, medical devices, agricultural biotechnology, and biomanufacturing. Professionals in this field may engage in research and development, quality control, clinical trials, regulatory affairs, or business development. Taiwan's biotech sector is known for its innovation and strong government support, offering opportunities in both startups and established companies. Careers range from laboratory research to management and marketing roles. The industry values scientific expertise, technical skills, and collaboration.

What are the key skills and qualifications needed to thrive in the Taiwan biotech industry, and why are they important?

To thrive in the Taiwan biotech industry, you typically need a solid background in life sciences or biomedical engineering, often with at least a bachelor's or master's degree. Familiarity with laboratory techniques, data analysis software, and regulatory compliance systems such as GMP is crucial. Strong problem-solving abilities, attention to detail, and teamwork enhance performance in dynamic research and development environments. These skills and qualifications are vital for driving innovation, ensuring product quality, and maintaining competitiveness in the rapidly growing biotech sector.

What is the difference between Taiwan Biotech vs Taiwan Biotech Research Associate?

AspectTaiwan BiotechTaiwan Biotech Research Associate
Required CredentialsBachelor's or Master's in Life Sciences, Biotechnology, or related fieldsBachelor's or Master's in Life Sciences, Biotechnology, or related fields
Work EnvironmentLaboratories, research facilities, production plantsLaboratories, research facilities, quality control labs
Employer & Industry UsageBiotech companies, pharmaceutical firms, research institutesBiotech companies, research labs, quality assurance departments

Both roles typically require similar educational backgrounds and work in biotech environments. However, Taiwan Biotech often refers to the industry or company as a whole, while Taiwan Biotech Research Associate is a specific job position focused on research and development tasks within the biotech sector.

More about Taiwan Biotech jobs
What cities are hiring for Taiwan Biotech jobs? Cities with the most Taiwan Biotech job openings:
What states have the most Taiwan Biotech jobs? States with the most job openings for Taiwan Biotech jobs include:
What job categories do people searching Taiwan Biotech jobs look for? The top searched job categories for Taiwan Biotech jobs are:
Taiwan Biotech jobs near you
Infographic showing various Taiwan Biotech job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 97% Full Time, and 2% Part Time. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution.

Senior Clinical Data Manager

Everest Clinical Research

Bridgewater, NJ • On-site, Remote

$90K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago

Job description

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that's us...that's Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Clinical Data Managers for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
Key Accountabilities:
Lead Data Management Activities, Perform Training and Client Relationship Management
  1. Develop and maintain Data Management Project Plan (Plan). Document deviations from the Plan, log and report issues, and follow up on their resolutions.
  2. Is the primary contact person for day to day data management activities, and is the person ultimately responsible for all data management deliverables for assigned projects.
  3. Is the primary contact person for communication and discussion of topics related to data management timelines and deliverables; request for out of scope tasks; first line contact for technical or procedural issues.
  4. Is responsible for planning and implementing data management timelines and deliverables; and is responsible for providing database and data management activities status reports; contributes to the overall project planning, progress tracking and reporting.
  5. Assist with study-level resource planning and management, including the review of team members' timesheet reports.
  6. Assist in performing client relationship management activities. Participate in project bid defense meeting when required.
  7. Perform training on electronic data capture (EDC) system, dataflow and quality control processes to clinical trial personnel.
  8. Provide training to new data management personnel on data management processes and procedures. Perform QC review of work performed by less experienced data management personnel.
  9. Assist in generation of project Work Orders and Amendments.
  10. Assist in management of dataflow from and performance of Third Party Vendors (Non-CRF data vendors).
  11. Participate in project kick off meeting, investigators meeting, and regular project management team meeting.
  12. Provide support to client audits and regulatory inspections. Follow up on audit findings.
  13. Create and maintain clinical trial Data Management Study Binders.

Perform Hands-on Data Management Activities
  1. Design and review case report forms (CRFs/eCRFs). Develop and review Case Report Form Completion Instructions. Generate and review annotated Case Report Forms.
  2. Design and review Clinical Trial Source Document templates and completion instructions when required.
  3. Develop and maintain data validation specifications.
  4. Develop and maintain Data Management Plan (DMP). Document deviations from the DMP.
  5. Participate in the database design process. Participate in EDC User Acceptance Testing (UAT).
  6. Manage the process of database modifications (after go-live) due to protocol amendments or study needs.
  7. Develop and maintain Data Quality Review Plan (DQRP). Coordinate with programmers to complete the programming and validation of the listings and summary tables as specified in the DQRP.
  8. Perform Third Party non-CRF data management activities.
  9. Review data, issue and resolve queries. Assist Investigative Site personnel with resolving queries.
  10. Perform Serious Adverse Event reconciliation.
  11. Assist in resolving medical coding discrepancies resulting from coding of medical history, adverse events, procedures and medicinal products.
  12. Cooperate and assist the Quality Assurance Department with quality control audits on assigned databases.
  13. Perform database soft-lock and hard lock activities.
  14. Maintain and prepare final archival of data management documentation relevant to the assigned clinical trials, and assist the corporate archivist in assembling and archiving such documentation.

Qualifications and Experience:
  1. A Bachelors' or Master's degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields.
  2. At least 5 years of experience in pharmaceutical clinical trial data management or at least 2 year of experience as a Clinical Data Manager II, with demonstrated knowledge, experience and ability to perform to meet high quality standards and high level of customer satisfaction.
  3. Demonstrated an in-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management, as well as pharmaceutical clinical trial regulations, industry guidance, conventions and standards
  4. Demonstrated a strong leadership in clinical data management activities and a desire to excel in leading data management projects.

Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a 401(k) retirement / pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $90,000 - $130,000.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
#LI-Remote
#LI-KD1
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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