← 返回岗位列表美国医疗健康与生命科学fulltime

Clinical Trial Project Manager

雇主

WEP Clinical

地点

美国

待遇

$0

工作模式

远程

🤖 AI 简历匹配评估

检测你的简历与该岗位的匹配度,免费

免费评估

岗位摘要

Are you looking for an exciting and fulfilling new position?

岗位职责

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives.Role Objectives:
The Clinical Project Manager at WEP Clinical is responsible for the setup, implementation, and management of clinical trials, ensuring patient safety, data integrity, and high-quality delivery in compliance with applicable regulations.
This role provides leadership across cross-functional teams, manages client relationships, and is accountable for delivering clinical trials on time, within scope, and within budget.
The Ideal Candidate:
Adaptable
Detail-oriented
Collaborative
Solutions-focused
What You'll Do:
The level of appointment (e.g., Project Manager II or Senior Project Manager) will be determined based on the candidate’s experience, skills, and demonstrated capabilities during the interview process.
Principal Dutiesand Responsibilities
Lead the setup, execution, and close-out of clinical trials in compliance with WEP Clinical SOPs, GCP/ICH guidelines, and regulatory requirements.
Provide day-to-day accountability for the operational delivery of assigned clinical trials.
Develop and maintain study manuals, operational project plans, timelines, and key performance metrics.
Ensure proper setup, maintenance, and close-out of eTMF and CTMS systems.
Leadership & Cross-Functional Oversight
Serve as project team lead and primary point of contact for internal and external stakeholders.
Provide oversight and coordination of cross-functional deliverables including monitoring, site management, data management, pharmacovigilance, regulatory, IP supply, and medical writing.
Ensure internal and external teams are appropriately trained on study protocols and operational requirements.
Client & Stakeholder Management
Act as the primary client contact for clinical trial operations, deliverables, and issue resolution.
Lead internal and external meetings, ensuring alignment on project status, risks, and timelines.
Risk & Issue Management
Identify, assess, and proactively manage risks and issues throughout the clinical trial lifecycle.
Implement mitigation strategies and corrective actions where required.
Regulatory & Compliance
Oversee submissions to IRB/ECs and review informed consent forms as required.
Ensure compliance with regulatory requirements and internal quality standards.
Collaborate with Quality Assurance to support audits, CAPAs, and investigations as appropriate.
Financial & Vendor Management
Manage project budgets, scope, and financial performance.
Oversee vendor performance and deliverables, including review and approval of invoices.
Review site payments and ensure alignment with Clinical Trial Agreements.
Documentation & Systems
Maintain accurate and complete trial documentation within internal systems (e.g., SharePoint).
Ensure all trial records meet quality and compliance standards.
What You'll Need:
Bachelor’s Degree(health or science field preferred)
Minimum 5 years’ experience in a Project Manager role within clinical trials or clinical research
Demonstrated experience managing clinical trials from initiation through close-out
Strong working knowledge of ICH GCP guidelines and clinical trial processes
Proven ability to lead cross-functional teams and manage multiple priorities
Strong organizational, problem-solving, and decision-making skills
Effective verbal and written communication skills
Proficiency in Microsoft Office tools
Ability and willingness to travel as required for business needs
Additional Notes
This role may be filled at different levels depending on experience and demonstrated capability.
Responsibilities may expand in scope with increased seniority and complexity of assigned projects.
Location eligibility applies. Candidates must reside in a U.S. state where the company is authorized to hire. This role is not eligible for residents of: California, Colorado, New York, Washington, New Jersey, Massachusetts, Illinois, Hawaii, and District of Columbia.
What We Offer:
Medical, dental, and vision insurance
FSA, HSA
Voluntary CriticalIllness, Hospital Indemnity, and Accident Insurance
Group short-term and long-term disability insurance
Group LifeInsurance
401K safe harbor plan and company match
Paid vacation, holiday, sick and volunteer time
Paid maternity & paternity leave
What Sets Us Apart:
WEP Clinicalpartners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalized service of a specialized provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.
We're Committedto Our Team:
WEP has many initiatives to encourage wellness, growth and development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events and all we do to support our employees.
How We Work at WEP Clinical:
At WEP Clinical, we look for individuals who are conscientious, exercise sound judgment, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives - and we are committed to helping our people grow and succeed in an inclusive, supportive environment.
Our Services Include:
Access Programs
Clinical TrialServices
Patient SiteSolutions
Clinical TrialSupply
Market Accessand Commercialization
Data PrivacyNotice:
WEP Clinicalis committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.
Privacy Policy:
Job Applicant PrivacyNotice:
How to Apply:
To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn’s Easy Apply option. Please ensure your resume is in English.
Important Note:
To streamline our hiring process, we use an Upwage AI screener. If you receive a link from Upwage, it is a legitimate part of our application process and helps ensure every candidate is reviewed consistently. If you are selected to move forward after the screener, a member of our team will contact you directly from an @wepclinical.com email address to guide you through the next steps of the interview process. Please ensure you apply only through our official careers page () or our verified LinkedIn page.
For Your Safety, Please Note:
We will nevercommunicate with you via Microsoft Teams or text message.
We will neverask for your bank account information at any stage of recruitment.
WEP Clinicalis a smoke-free, drug-free, and alcohol-free work environment.
WEP Clinicalis an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.
Originally posted on Himalayas

申请条件

- Proven experience in clinical trial management, including setup, execution, and close-out
- Strong knowledge of GCP/ICH guidelines and regulatory requirements
- Familiarity with SOPs and clinical research operations
- Experience with eTMF and CTMS systems
- Ability to lead cross-functional teams and manage client relationships
- Skilled in developing project plans, timelines, and performance metrics
- Excellent organizational, communication, and problem-solving skills
- Adaptable, detail-oriented, collaborative, and solutions-focused mindset
- Relevant educational background (e.g., life sciences, nursing, or related field)
- Demonstrated capability to manage trials on time, within scope, and budget

雇主简介

WEP Clinical 是一家专注于临床研究的组织,负责临床试验的设立、实施和管理,以确保患者安全和数据完整性。

对这个岗位感兴趣?

该岗位暂未开放在线申请,顾问可为您推荐同类岗位或申请指导

咨询不收取任何费用,顾问将为您推荐合适的岗位与申请方式

申请海外岗位,英文简历符合当地格式规范吗?

AI 自动评估你与该岗位的匹配度,3 分钟出结果

免费评估简历匹配度

数据来源:Himalayas

岗位信息来源于公开渠道,版权归原作者所有