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China JOBS - Covance

Study Coordinator- BioA LM Shanghai, China

Job Overview Independently performs activities related to Project management process by coordinating activities for routine studies in compliance with appropriate protocol, Standard Operating Procedures (SOPs) and regulatory agency guidelines, in a timely, efficient, and quality manner. 1. Essential Job Duties: * Independently drafts protocols, sample analysis outlines (SAOs), amendments and st . . Read More

Senior Proposal Manager Shanghai, China

Job Overview * Is accountable and provides leadership for all aspects of the appropriate proposal/budget process (text, quote, budget, and/or response to Requests for Information [RFIs] * May leads strategic and/or highly complex opportunities and/or initiatives * Is accountable for assigned team workload management, monitoring team capacity, and assisting in priority setting * Triages and assign . . Read More

Sales Associate Shanghai, China

Job Overview * Close daily working relationship with Business Development Directors in Covance China Early Development to ensure that all client needs/expectations are being attended to at all times * Work with/assist Business Development Directors in providing requested proposals to clients on a timely basis and be in a position to respond to any questions raised by clients * Work with/assist Bu . . Read More

Data Mgr II Shanghai, China

Job Overview 1. Engage client data management during start up. * Create protocol folder(s) for study documentation. * Add entries into individual protocol spreadsheet. * Review Statement of Work (SOW) for study scope. * Ensure start-up packet delivery to clients. * Contact clients for initial study discussion and determine authors of Data Transfer Specifications (DTS). * Provide recommendations . . Read More

Research Assistant-Formulation Shanghai, China

Job Overview * Promotes a cohesive team environment. * With supervisory assistance, assures technical staff compliance to SOPs and other regulatory agency guidelines. * Assists in setting up and performing method development and validation of various analytes * in a variety of matrices. * Performs complex analyses using unfamiliar or new methods, asking for scientific guidance as needed. * Writes . . Read More

EA & Office Admin Shanghai, China

Job Overview * Manage the site management team's schedule and coordinate all travel-related activities * Organize travel and hotel bookings for the site management team and designated departments * Assist visitors to Shanghai with accommodation, set up office, calendar, events, etc. * Coordinate with relevant departments and consolidate the site monthly report * Organize and schedule internal and . . Read More

Animal Lab Testing PI Shanghai, China

Job Overview 1. Mainly focus on clinical laboratory testing for non-Tox studies accurately and in a timely manner. 1. Work with sponsor on assay development. Resolve routine and non-routine assay problems. 2. Retrieve and check specimens against pending list. Document and resolve any specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved. 3. Prepare work . . Read More

GLSS Administrator- 实验室运营管理方向 Shanghai, China

Job Overview General Duties and responsibility * Responsible for policies, procedures, and maintenance required to support all systems and applications owned and managed by GLSS * Provide back up to GLSS Coordinator * Provide support for training when needed for new GLSS Coordinator * Based on business need, may be assigned tasks at level above (GLSS Administrator I) * Monitor and report perf . . Read More

AD Employee Relations Shanghai, China

Job Overview * Manages and leads the team in their location, ensuring minimal attrition, full team engagement and creativity to bring out the best in their direct line reports. * Displays an understanding of complex team dynamics to ensure the ER team grows, gets stronger and manages change effectively. * Continually looking for opportunities to improve ER, make it more effective and maintain the . . Read More

Sr. Medical Director / Medical Director - Oncology Beijing, China

Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to serve as a physician providing subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Sr. Medical Director will play a key role in people leadership/management, client relations, . . Read More

Sr. Medical Director / Medical Director - Oncology Shanghai, China

Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to serve as a physician providing subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Sr. Medical Director will play a key role in people leadership/management, client relations, . . Read More

Recruitment Manager, FSPx Shanghai, China

Job Overview - Recruiting partner to FSPx business, collaborating with hiring teams, HR, and recruitment process outsourcing provider to provide recruiting solutions to business needs. Proactively engages in workforce planning to create and implement custom recruiting strategies aligned to global processes. - Manages full-cycle recruitment activity (sources, screens and secures candidates) for . . Read More

Logistics Specialist I Shanghai, China

Job Overview * Be responsible for communicating with PI/PMs to prepare all the import/export permits. E.g. CIQ risk assessment, CITES, CFDA, etc * Be responsible for Customs clearance for the shipments * Be responsible for the domestic shipments * Checking billing list and finishing check requests for Logistics related vendors monthly. * Document all transportation service failures, resolve, . . Read More

Proj Mgr Drug Safety Beijing, China

Job Overview * Provide leadership and management of global or regional projects ensuring that communications and processes are harmonized for assigned projects. - Monitor and manage the workflow for assigned projects to ensure all deadlines are met and compliant safety reporting in accordance with International reporting regulations, Standard Operating Procedures (SOPs) and safety processing gui . . Read More

Proj Mgr Drug Safety Dalian, China

Job Overview * Provide leadership and management of global or regional projects ensuring that communications and processes are harmonized for assigned projects. - Monitor and manage the workflow for assigned projects to ensure all deadlines are met and compliant safety reporting in accordance with International reporting regulations, Standard Operating Procedures (SOPs) and safety processing gui . . Read More

Proj Mgr Drug Safety Shanghai, China

Job Overview * Provide leadership and management of global or regional projects ensuring that communications and processes are harmonized for assigned projects. - Monitor and manage the workflow for assigned projects to ensure all deadlines are met and compliant safety reporting in accordance with International reporting regulations, Standard Operating Procedures (SOPs) and safety processing gui . . Read More

Mgr Drug Safety Dalian, China

Job Overview * Responsible for the line-management of individuals within a team as well as a project team. * Manage direct reports to ensure staff training records are up to date. * Responsible for managing performance reviews and issues of direct reports. * May manage individuals across multiple teams and will take on responsibility for cross department projects. * Responsible for office managem . . Read More

Clin Data Coord I Dalian, China

Job Overview - Review clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs, Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data - Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data - Ge . . Read More

Clin Data Coord I Dalian, China

Job Overview - Review clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs, Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data - Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data - Ge . . Read More

Clin Data Coord I Dalian, China

Job Overview - Review clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs, Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data - Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data - Ge . . Read More

Statistical Programmer 1 Dalian, China

Job Overview * Provide Statistical Programming service * Develop and review SAS programs and output for the management and reporting of clinical trial data including ADaM and client-defined analysis datasets, tables, listings and graphs. * Develop programs for data transfers and assist in their review to ensure the data transfer has been produced to specification * Review draft and final producti . . Read More

Sr Mgr Regional Qual Control Shanghai, China

Job Overview Reporting to the Director Global Quality Control, this Senior Manager, Regional Quality Control (SMRQC) position will work primarily with Clinical Operations and Project Management and with other Functions as appropriate to ensure that the contract specified activities conducted by these departments meet or exceed all obligations defined by the project contract. In addition, this ind . . Read More

GLP QA Officer I Shanghai, China

Job Overview * Performs protocol, data, report, and in-lab phase inspections for a specific study type to verify conformance to applicable SOP and regulatory requirements.- * Evaluates responses to inspection reports and performs follow-up with respondents, management, or others, if needed, to ensure resolution.- * Ensures that systems used in QA are properly maintained (e.g., QA audit records, t . . Read More

GLP QA Officer I Shanghai, China

Job Overview * Performs protocol, data, report, and in-lab phase inspections for a specific study type to verify conformance to applicable SOP and regulatory requirements.- * Evaluates responses to inspection reports and performs follow-up with respondents, management, or others, if needed, to ensure resolution.- * Ensures that systems used in QA are properly maintained (e.g., QA audit records, t . . Read More

Proposal Administrator Shanghai, China

Job Overview 1. Essential Job Duties: * These statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. These are the specific areas of accountability requiring decisions or delivery of results. * Provides administrative support to the Proposal Management team (e.g. photocopying, assistance with qu . . Read More

Global Study Manger I Shanghai, China

Job Overview Essential Job Duties: * Key contact for clients; Liaison between Clients, CRO, and Covance * Displays leadership to ensure successful interactions between Covance study team members needed to provide seamless study delivery to the client. * Provides project management oversight; focusing on key client deliverables through budget, risk, and milestone management. * Facilitates comm . . Read More

Clinical Research Associate II Guangzhou, China

Job Overview Are you a Clinical Research Associate who wants to work with one of leading global CROs in the industry? Covance is seeking CRAs with at least 1 year clinical monitoring Experience NATIONWIDE, and has a variety of CRA needs in Phase II-IV and Phase I (Early Clinical Development) in multiple therapeutic areas such as oncology, cardiovascular, diabetes mellitus, endocrinology, etc. Wh . . Read More

Project Manager Drug Safety Shanghai, China

Job Overview In your role as Project Manager Drug Safety you will * Provide leadership and management of global or regional projects ensuring that communications and processes are harmonized for assigned projects. * Monitor and manage the workflow for assigned projects to ensure all deadlines are met and compliant safety reporting in accordance with International reporting regulations, Standard . . Read More

Clinical Research Associate II Guangzhou, China

Job Overview Are you a Clinical Research Associate who wants to work with one of leading global CROs in the industry? Covance is seeking CRAs with at least 1 year clinical monitoring Experience NATIONWIDE, and has a variety of CRA needs in Phase II-IV and Phase I (Early Clinical Development) in multiple therapeutic areas such as oncology, cardiovascular, diabetes mellitus, endocrinology, etc. Wh . . Read More

Senior Auditor II Beijing, China

Job Overview * Leads the conduct, reporting and follow up of regional and local QA audits, ensuring compliance to applicable SOPs, Master Audit Plan, and within specified timeframes and quality standards * Conducts complex, directed, and/or time sensitive QA audits * Participates in global QA audits * Provides suitable recommendations for audit observations; ensures auditees deliver appropriate C . . Read More

Medical Director Beijing, China

Job Overview Reporting to the Vice President and Global Therapeutic Area Head (Neurology, Ophthalmology, and Women's Health), the primary role of the incumbent will be to serve as the global lead physician providing subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Sr. Medical . . Read More

Medical Director Shanghai, China

Job Overview Reporting to the Vice President and Global Therapeutic Area Head (Neurology, Ophthalmology, and Women's Health), the primary role of the incumbent will be to serve as the global lead physician providing subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Sr. Medical . . Read More

Medical Director Beijing, China

Job Overview Reporting to the Vice President and Global Therapeutic Area Head of Inflammation, Infectious Diseases & General Medicine (iiGM), the primary role of the incumbent will be to serve as the lead physician providing subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Me . . Read More

Medical Director Shanghai, China

Job Overview Reporting to the Vice President and Global Therapeutic Area Head of Inflammation, Infectious Diseases & General Medicine (iiGM), the primary role of the incumbent will be to serve as the lead physician providing subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Me . . Read More

Proj Mgr IV Shanghai, China

Job Overview Lead core project teams and facilitate team's ability to lead extended/complete project team(s). Depending on the size and scope of project(s) ensuring effective cross-functional teamwork among project team members including both internal and external stakeholders. The PM Job duties may be performed in collaboration with a senior project manager and/or Project Director. Provide proj . . Read More

Sr Assoc Drug Safety Beijing, China

Job Overview Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: * entry of safety data onto adverse event database(s) and tracking systems * review of adverse events for completeness, accuracy and appropriateness for expedited reporting * write patient narratives * code adver . . Read More

Sr Assoc Drug Safety Dalian, China

Job Overview Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: * entry of safety data onto adverse event database(s) and tracking systems * review of adverse events for completeness, accuracy and appropriateness for expedited reporting * write patient narratives * code adver . . Read More

 

Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit www.gettinghired.com or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).