This role is for upcoming future opportunities that may arise at Fortrea. Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interv…
Career CategoryRegulatoryJob Description Job Description Applying, obtaining and maintaining regulatory approvals for products within Amgen’s portfolio, including CTN, MAA, renewal, variations of product’s life cycle man…
Key Responsibilities: Integrated Hemophilia Platform Strategy and OperationsLead the development and execution of the Hemophilia integrated platform strategy to shape the rare disease policy, improve affordability, and u…
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less in…
Skills: Business Behavior, Communication, Consulting, Cross-Selling, Customer Centricity
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to p…
Job Description Job Responsibilities: 1- Build and maintain good communication with central government stakeholders including National Healthcare Security Administration (NHSA) and related government agencies. 2- Monitor…
Background Sanofi has decided to invest in new, state-of-the-art production facilities for the entire insulin portfolio as part of the InsuLINK program, to ensure a future-oriented, sustainable, and reliable long-term su…
INTRODUCTORY PARAGRAPH Evinova is a health-tech business, accelerating the delivery of better health outcomes by propelling the life sciences sector forward in digital health, from the inside. Evinova delivers proven out…
Skills: Clinical Outcomes Assessments, Outcomes Research, Patient-Reported Outcomes, Digital Health, Qualitative Research
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every …
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every …
Skills: Product Knowledge, Disease Area Expertise, Market Strategy Execution, HCP Relationship Management, Customer Data Management
Clarivate is a global leader committed to innovation and collaboration, offering an environment where you can thrive both professionally and personally. We are looking for great Renewal Account Managers to join our team …
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: Medical Marketing Strategy, Medical Review, KOL Relationship Management, Clinical Data Integration, Medical Education
Job Title: Regulatory Affairs Manager, I&I Alliance Reports to: TA Head, I&I Alliance, China Team Management: Individual Contributor Key Responsibilities: China – I&I Alliance Support the development and implementation o…
Senior Director & Asia Pacific Regional Lead, External R&D
Beijing, Beijing, China · On-site
Senior$9.7B raised
About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to…
Skills: Search & Evaluation, Business Development, Stakeholder Engagement, Partnerships Governance, Technical Due Diligence
CRA, China ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaborati…
Skills: Clinical Trial Monitoring, Site Qualification, Protocol Compliance, Data Integrity, Patient Safety
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical de…
Skills: Program Management, Line Management, Clinical Operations, Resource Management, KPI Tracking
Essential Functions • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as neces…
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Full-time
bachelor degree, professional certificate, postgraduate degree
Posted 19d ago
~40 hrs/week
Remote in Beijing, Beijing, China
Responsibilities
The Project Manager is responsible for the operational strategy, budget, and timely delivery of clinical trials while maintaining quality and customer satisfaction. They lead high-performing teams in a matrixed environment to manage the end-to-end project lifecycle from scope to execution.
Requirements
Requires a university degree in life sciences or allied health and at least five years of clinical research experience in a pharmaceutical or CRO setting. Proficiency in ICH/GCP guidelines and advanced computer skills are essential, with PMP certification and a Master's degree preferred.
Full job description
This role is for upcoming future opportunities that may arise at Fortrea.
Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving forward with an offer.
Job Overview:
Project Managers own the operational strategy, determining the most cost effective and efficient means to successfully run and complete projects on time, while maintaining quality, remaining within budget, while meeting the customer’s needs and adhering to the contract. Project Managers will work to develop and lead high performing teams by collaborating with key stakeholders to manage all aspects of the end-to-end lifecycle of the project including scope, timelines, risk, and budget. A successful Project Manager will bring innovation and future focused approaches to clinical trials with a focus on patient centricity and consistent solutions-oriented delivery.
Summary of Responsibilities:
Take accountability for proactively driving project performance toward contracted deliverables while meeting customer needs and maintaining operational excellence.
Take ownership of the customer relationship while drawing on the Company’s pool of experts.
Drive communication and collaboration with the client and project team across a matrixed, multi-cultural, environment. Lead the development of the project strategy and ensure prioritization with the project team and key stakeholders in the creation of clear, data driven strategies and proactive management of project scope, timelines, quality, and budget. In collaboration with relevant departments, prepare and deliver presentations for new business as required.
Lead the identification of project, financial and quality risk leveraging end to end risk management practices and quality by design principles. Appropriately utilize data sources, dashboards, and risk management strategies to drive innovation and proactive problem solving with the project and client teams. Lead the adherence to project governance and issue escalation pathways, ensuring that project plans are in place to address identified risk while adhering to professional standards, SOPs, client, and regulatory requirements.
Partner with project team members and key stakeholders to oversee and manage project budgets, resources, and scope. Ensure adherence to established budget and financial milestones. Accountable for accurately forecasting project revenue and managing project costs in adherence to the budget. Leading the timely management of changes to scope and the change order process. Ensures project team awareness and tracking of KPIs for any client specific metrics.
Provide inspiring leadership and play a key role in the creation of high performing project teams. Facilitating communication and teamwork while driving delivery, ensuring that team members understand contracted scope, timelines, and budget. Ensures that resource projections are accurate and visible to resourcing teams, proactively escalating resource constraints and challenges. Develops and mentors team members in multiple areas of expertise and provides feedback as needed to respective line managers.
All other duties as needed or assigned.
Qualifications (Minimum Required):
University/college degree (life science preferred) or certification in a related allied health profession (i.e., nursing, medical or laboratory technology) from an appropriately accredited institution.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Experience (Minimum Required):
Minimum of five (5) years of relevant clinical research experience in a pharmaceutical company/CRO.
In lieu of the above requirement, candidates with (a) six (6) years supervisory experience in a heath care setting and (b) five (5) years clinical research experience including one (1) years of project management experience (international clinical trial management experience preferred) in the pharmaceutical or CRO industries will be considered.
Preferred:
Experience in Project Management of the End-to-End Clinical Trial Lifecycle or
Project Management of large-scale Projects in other industries.
On the Job Experience:
Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, and Power Point).
Experience managing projects in a matrix and virtual environment.
Excellent communication, planning, and organizational skills.
Demonstrated ability to lead by example and to encourage team members to seek solutions independently.
Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
Financial awareness and ability to actively utilize financial tracking systems.
Ability to work independently and mentor junior project team members.
Ability to negotiate and liaise with clients in a professional manner.
Ability to present to staff at all levels.
Preferred Qualifications Include:
Master’s or other advanced degree.
Minimum of five (5) years of relevant clinical research experience in a pharmaceutical company/CRO.
In lieu of the above requirement, candidates with (a) six (6) years supervisory experience in a heath care setting and (b) five (5) years clinical research experience including one (1) years of project management experience (international clinical trial management experience preferred) in the pharmaceutical or CRO industries will be considered.
Experience in Project Management of the End-to-End Clinical Trial Lifecycle or Project Management of large-scale Projects in other industries.
On the Job Experience:
Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, and Power Point).
Experience managing projects in a matrix and virtual environment.
Excellent communication, planning, and organizational skills.
Demonstrated ability to lead by example and to encourage team members to seek solutions independently.
Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
Financial awareness and ability to actively utilize financial tracking systems.
Ability to work independently and mentor junior project team members.
Ability to negotiate and liaise with clients in a professional manner.
Ability to present to staff at all levels.
PMP certification
Master’s or other advanced degree.
Physical Demands/Work Environment:
Standard Office Environment or remote based work required.
Weekend and off-hour work as required.
Travel Requirements:
Local, Domestic, Regional, Global
Identify the expected travel requirements of the position on an annual basis:
% of time: up to 30%
% of the above that requires overnight stay: up to 30%
Travel is primarily to where: domestic and international travel
Bringing life-changing benefits to patients faster
Industry
Biotechnology Research
Company size
10,001+ employees
Headquarters
Research Triangle Park, NC
LinkedIn followers
257,542
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.
Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.
Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.
Together, exceptional is possible.
Learn more at Fortrea.com
Offices: Research Triangle Park, NC, US
clinical researchclinical trialsand medical device trialsHealth CareClinical Trials
How many Healthcare jobs are open in Beijing, China right now?
There are currently 544 open healthcare positions in Beijing, China listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Beijing, China?
Companies currently hiring include Sanofi, IQVIA, Takeda, GE HealthCare, ICON plc, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Beijing, China?
Yes — 109 of the 544 open healthcare positions offer remote or hybrid work (34 remote, 75 hybrid).
How do I apply for Healthcare jobs in Beijing, China?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.