波兰语可行性专员 - FSP
Feasibility Specialist with Polish - FSP
当我们的价值观一致时，我们能够实现无限可能。
在Parexel，我们都有相同的目标——改善全球健康。从临床试验到监管、咨询和市场准入，我们提供的每项临床开发解决方案都源于一种特别的信念——对我们所做工作的深刻认同。
无论我们在Parexel做什么，都在为最终惠及患者的疗法开发做出贡献。我们认真对待工作，带着同理心去做，并致力于带来改变。
关于Parexel
Parexel是领先的全球临床开发合作伙伴，为生命科学行业提供以洞察为导向的临床和咨询服务。全球拥有22,000多名员工，我们与生物制药公司和研究机构合作，设计并实施以患者为中心的临床试验，扩大访问范围，使研究成为任何地方任何人的治疗选择。
我们专注、敏捷且有共同目标地工作，迅速响应患者需求，加速新疗法的交付。我们鼓励大胆思考，快速适应变化，并持续提高临床研究的速度和质量。我们正在扩大团队，寻找有才华的人士来推动行业领先创新，用心做事。
岗位职责：
· 作为区域情报团队的支持成员
- 执行多个站点情报和可行性项目任务
- 能够管理大量复杂的试验和站点
- 在区域情报团队主管的密切监督下工作，必要时与可行性专家联系人（POC）协作
- 参与执行站点可行性计划，并向同事展示数据
- 协助可行性策略与分析负责人（FSAL），确保理解站点可行性项目的总体目标、范围和要求，并确保高质量的结果被执行和交付
- 将技能和专业知识应用于OARS和区域情报开发项目
- 推动持续改进文化，优化流程以提高效率和生产力
- 开发和维护内部流程，以优化国家和站点选择活动
- 通过作为跨职能团队领导者工作，向广泛的利益相关者传达数据、分析和区域站点情报计划，提高意识
查看英文原文
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 development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About Parexel
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose - moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart.
Role Responsibilities:
· Acts as a supportive team member for Regional Intelligence
- Performs tasks for multiple Site Intelligence and Feasibility projects.
- Able to manage a high volume of complex studies and sites
- Works under close supervision of Regional Intelligence Team Lead, and where needed the Feasibility Specialist Point of Contact (POC)
- Contributes to executing Site Feasibility plans and presenting the data to colleagues.
- Supports the Feasibility Strategy & Analytics Lead (FSAL) to ensure knowledge of goals, scope and requirements of the Site Feasibility project are understood, and ensures that high quality results are executed and delivered.
- Applies skills and discipline knowledge to OARS and Regional Intelligence development projects
- Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity
- Develops and maintains internal processes aimed to optimize country & site selection activities
- Creates awareness by working as a cross functional team leader to deliver data, analytics and regional site intelligence initiatives across a broad spectrum of stakeholders, both internal and external
- Contribution to wider initiatives, both technology and process improvement components
- Runs operational and technical aspects of large global projects and assists with other Company systems activities related to site intelligence
- Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitates effective portfolio delivery
- Partners with GSSO and CD&O teams to improve overall study start up metrics and implement simple processes
BASIC QUALIFICATIONS
- In general, candidates for this job would have the following levels of experience in Clinical Research/Clinical Operations: 2-3 years
- Fluent in English and Polish
- Manager/Senior Associate: Experience working in the pharmaceutical industry or CRO in a similar role
- Effective verbal and written communication skills in relating to colleagues and stakeholders both inside and outside of the organization
- Strong presentation skills, interpersonal skills, as well as a team oriented approach. Excellent verbal, written, communication and time management skills
- Ability to multitask under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high quality work
PREFERRED QUALIFICATIONS
· Experience in a clinical research organization and related therapeutic specialties with familiarity in principles, concepts, practices and standards.
- Prior feasibility experience
- An eye for detail and ability to problem solve operational challenges and provide high level insights to a multidisciplinary team.
- Proficiency in Microsoft SharePoint
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, database applications)
- A quick learner with the desire to contribute and support the design and implementation of analytical insights and management of data platforms.
- Demonstrated success/results in prior roles including matrix organization
Organizational Relationships:
· Collaborates across functional lines within CD&O, R&D, Contract Research Organizations (CROs), Legal and Quality Representatives, and Functional Service Providers (FSPs).
- Works under supervision of Regional Intelligence Team Lead
- Global Study Manager, Start-Up Project Manager, Global Study Clinician
- Local Site Relationship Partners and Director Clinical Site Operations (DCSO), Clinical Trials Manager and other Local Roles
- Global Quality and Event representatives
- Feasibility Strategy & Analytics Lead (FSAL) & Due Diligence Lead
Originally posted on Himalayas