临床研究助理
Clinical Research Associate
临床研究助理（居家办公，巴塞罗那）
ICON是一家全球医疗智能和临床研究组织，致力于更快地为患者带来新药和治疗方法。
作为一家以价值观驱动的组织，诚信、协作、敏捷和包容是我们工作和与彼此、客户、患者及供应商互动的核心。
在ICON担任CRA II职位，您将设计和分析临床试验，解读复杂的医学数据，并为创新治疗和疗法的进步做出贡献。
您将参与临床试验监查活动，对您的交付成果负责并进行协作。
主要职责包括：
- 进行临床试验的现场评估、启动、监查和结束访问。
- 在整个试验过程中确保方案符合性、数据完整性和患者安全。
- 与研究者和现场工作人员合作，确保研究顺利进行。
- 执行数据审查和问题解决，以保持高质量的临床数据。
- 参与研究文件的准备和审核，包括方案和临床研究报告。
您的背景：
您将具备相关的临床试验监查经验，以及以下资格和技能。
所需资格和经验：
- 科学或医疗相关领域的学士学位。
- 至少2年的临床研究助理工作经验。
- 精通临床试验流程、法规和ICH-GCP指南。
- 强大的组织和沟通能力，注重细节。
- 能够在快节奏环境中独立和协作工作。
- 根据需要愿意出差（约60%）
在ICON就业取决于您是否拥有在该职位所在国家合法工作的权利。
奖励与福利
ICON提供具有竞争力且全面的总薪酬包，旨在支持您的健康、福祉和职业发展。
福利可能包括：
- 具有竞争力的基本薪资和绩效相关激励
- 健康和福祉计划，包括医疗、牙科和视力保险（适用地区）
- 退休和养老金计划
- 寿命保障和残疾保险
- 员工援助计划和福祉资源
- 通过结构化培训提供的学习和发展机会
查看英文原文
Clinical Research Associate Home based Barcelona
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, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a CRA II 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