Clinical Research Associate
临床研究员 II/CRA II - （疫苗）- （远程 - 保加利亚）在 ICON 战略解决方案，你将在一个专注于赞助商的模型中工作，由 ICON 全球专业知识支持。作为世界上最大的 FSP 组织，拥有90多个赞助商合作伙伴关系，我们提供稳定性，职业发展和协作环境，其中你的工作可以为世界各地患者有益的治疗开发做出贡献。作为 ICON 的临床研究人员，你将设计和分析临床试验，解释复杂的医学数据，并促进创新治疗和疗法的进步。你将参与临床试验监测活动，负责你的结果并协同工作。主要责任包括：· 对临床试题进行现场合格，启动，监控和接近访问。·确保整个试验过程中遵守协议，数据完整性和患者安全。· 与调查人员和现场员工合作以促进流的研究行为。·执行数据审查和查询解决，以保持高质量的临床数据。· 贡献于准备和审查研究文档，包括议定书和临床研究报告。你将带来相关的临床试验监测经验，以及以下资格和技能。所需的资格和经验：· 在科学或医疗保健领域获得学士学位。· 作为临床研究助理工作至少2年的经验。· 深入了解临床试题过程，法规和 ICH-GCP 指导方针。· 有强大的组织和沟通能力，注意细节。·在快速发展环境中独立合作工作的能力。·随需要旅行愿意 （约60%）ICON 的就业取决于有合法权利在该角色所在的国家工作。奖励与福利 ICON 提供了一个具有竞争力的，全面的总奖励方案，旨在支持你的健康，福祉和职业发展。优势可能包括：· 竞争性基本工资和绩效相关激励措施 · 包括医疗，牙科和视觉覆盖的卫生和幸福计划，如有所需 · 年度退休和养老金计划 · 生活保险和残疾保险 · 员工援助计划和福利资源 · 学习
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Clinical Research Associate II / CRA II - ( Vaccines ) - Remote - BulgariaAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Clinical Research Associate at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high-quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Your Profile:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Willingness to travel as required (approximately 60%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
Originally posted on Himalayas