Clinical Data Coordinator II

Reposted 22 Days Ago
Be an Early Applicant
Manila, First District NCR, National Capital Region, PHL
In-Office
Mid level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
As a Clinical Data Coordinator, you will manage clinical data collection, ensure compliance, and collaborate with teams for quality data management.
Summary Generated by Built In
Clinical Data Coordinator - Homebased - PHL

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Clinical Data Coordinator to join our diverse and dynamic team. As a Clinical Data Coordinator at ICON, you will be responsible for overseeing the collection, management, and quality of clinical data to ensure compliance with regulatory requirements and project timelines. Your expertise will be vital in supporting the successful execution of clinical trials through effective data management practices.

What You Will Be Doing:

  • Coordinating data collection activities, ensuring accuracy and completeness of clinical trial data.
  • Managing data entry processes and performing quality control checks to maintain data integrity.
  • Collaborating with cross-functional teams, including clinical operations and data management, to address data-related issues and enhance project efficiency.
  • Assisting in the development and implementation of data management plans and standard operating procedures.
  • Staying current with industry trends and best practices in clinical data management to drive continuous improvement initiatives.

Your Profile:

  • Bachelor's degree in life sciences, data management, or a related field; advanced degree preferred.
  • Proven experience in clinical data coordination or management within the clinical research industry.
  • Strong analytical skills and attention to detail, with a focus on data accuracy and quality.
  • Excellent communication and interpersonal skills, facilitating effective collaboration with diverse teams and stakeholders.
  • Proficiency in data management systems and clinical trial management software.
  • A commitment to maintaining high standards of quality and compliance in all data-related activities.
  • Must be amenable to work homebased, midshift schedule (3pm-12mn PHT)

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family’s needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values.   We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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