SSU Group Leader at ICON plc

Beijing, Beijing, China -

Full Time

Start Date

Immediate

Expiry Date

19 Sep, 26

Salary

0.0

Posted On

21 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Start-Up, Clinical Operations, Team Management, Regulatory Compliance, ICH/GCP Guidelines, Stakeholder Management, Project Management, Leadership, Mentorship, Process Improvement, Clinical Trial Activation, Interpersonal Communication

Industry

Biotechnology Research

Description

SSU Group Leader, office based 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 SSU Group Leader at ICON, you will oversee the site start-up process for clinical trials, ensuring timely and efficient initiation of sites while maintaining compliance with regulatory requirements and company standards. What You Will Do: You will oversee site start-up and activation operations, balancing quality, timelines, and stakeholder expectations. Key responsibilities include: Leading and managing the SSU team to ensure timely activation of clinical trial sites and adherence to project timelines. Overseeing the preparation and submission of essential documents to regulatory authorities and ethics committees, ensuring compliance with local regulations. Collaborating with project managers and cross-functional teams to streamline processes and resolve issues related to site start-up activities. Developing and implementing best practices for site start-up operations, driving continuous improvement initiatives to enhance efficiency. Providing mentorship and professional development opportunities for SSU team members, fostering a culture of collaboration and excellence. Your Profile: You will have a strong background in site start-up and activation, with proven management experience and a commitment to quality delivery. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Significant experience in site start-up or clinical operations within the pharmaceutical or clinical research industry. Strong leadership and management skills, with experience in building and developing high-performing teams. Excellent understanding of regulatory requirements and processes related to site start-up, including ICH/GCP guidelines. Exceptional communication and interpersonal skills, with the ability to build relationships with internal and external stakeholders and drive successful project outcomes. Willingness to travel as required (approximately 25%) 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 ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

Responsibilities

Oversee the site start-up and activation process for clinical trials to ensure timely initiation and regulatory compliance. Lead the SSU team, manage essential document submissions, and collaborate with cross-functional teams to optimize operational efficiency.