临床科学项目专员 (100% 远程)
Clinical Science Program Specialist (100% Remote)
我们客户是诊断和生命科学领域的全球领先企业，现正在寻找一名“临床科学项目专员（100%远程）”。
工作时长：长期合同（可能续约）
薪资：35美元/小时（W2）
公司福利：医疗、牙科、视力、带薪病假、401K
协调和管理多个临床检测和实验室服务项目，从启动到完成，作为制药客户的首要联系人。推动跨职能项目执行，监督样本流程活动，并在受监管环境中确保临床研究结果及时准确地交付。
关键职责：
- 在项目经理的指导下，管理多个临床检测和实验室服务项目。
- 制定项目计划、时间表，并协调跨职能活动以确保按时执行。
- 监控项目进展，识别风险和瓶颈，并实施解决方案以保持里程碑。
- 监督样本处理流程并确保结果的准确报告。
- 作为制药客户、CRO、现场研究人员和内部利益相关者的首要联络人。
- 协调会议，准备议程，记录会议纪要，并传达项目更新。
- 跟踪并维护项目报告和临床研究数据。
- 在临床运营中推广最佳实践和持续改进。
资格要求：
- 需要学士学位；生命科学专业优先。
- 2年以上在CRO、诊断、制药或受监管行业中的项目协调、临床试验协调或项目管理经验。
- 接触过临床研究和受监管的文件。
- 具备出色的组织、沟通和协作能力。
- 能够在快节奏的环境中管理多个项目。
优先资格：
- 具有伴随诊断（CDx）、临床检测或生物样本管理的经验。
- 了解临床试验管理流程和PMI方法。
- 在诊断或制药行业有经验。
如感兴趣，请将更新的简历发送至
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最初发布于喜马拉雅山
查看英文原文
Our client, a worldleader in diagnostics and life sciences, is looking for a“ClinicalScience Program Specialist (100% Remote)".
Job Duration: LongTerm Contract (Possibility Of Extension)
Pay Rate : $35/hr on W2
Company Benefits:Medical, Dental,Vision, Paid Sick leave, 401K
Coordinate and managemultiple clinical testing and laboratory services projects from initiationthrough completion, serving as the primary point of contact for pharmaceuticalclients. Drive cross-functional project execution, oversee sample workflow activities,and ensure timely, accurate delivery of clinical study results in a regulatedenvironment.
Key Responsibilities:
- Manage multiple clinical testing and lab services projects under the guidance of the Program Manager.
- Develop project plans, timelines, and coordinate cross-functional activities to ensure on-time execution.
- Monitor project progress, identify risks and bottlenecks, and implement solutions to maintain milestones.
- Oversee sample processing workflows and ensure accurate reporting of results.
- Serve as the primary liaison for pharmaceutical clients, CROs, site investigators, and internal stakeholders.
- Coordinate meetings, prepare agendas, document minutes, and communicate project updates.
- Track and maintain project reports and clinical study data.
- Promote best practices and continuous improvement across clinical operations.
Qualifications:
- Bachelor’s degree required; Life Sciences preferred.
- 2+ years of project coordination, clinical trial coordination, or project management experience in the CRO, diagnostics, pharmaceutical, or regulated industry.
- Exposure to clinical studies and regulated documentation.
- Strong organizational, communication, and collaboration skills.
- Ability to manage multiple projects in a fast-paced environment.
PreferredQualifications:
- Experience with companion diagnostics (CDx), clinical testing, or biosample management.
- Knowledge of clinical trial management processes and PMI methodologies.
- Experience within the diagnostics or pharmaceutical industry.
If interested, pleasesend us your updated resume at
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Originally posted on Himalayas