Publications and Scientific Communications Lead
At a glance
Senior Communications role at ICON. US, Blue Bell (PRA) · full-time.
Pay not stated Communications Lead salary
growthroles summary, based on the employer's posting.
What you'll do
- Run clinical research projects, keeping scientific work aligned with study protocols and delivery schedules
- Shape research plans with cross-functional colleagues and work through scientific problems as they arise
- Guide study design, execution and analysis, with attention to reliable data collection and interpretation
- Advise teams on research methods, data analysis and regulatory compliance throughout project work
- Build working relationships with research partners and regulators to move project objectives forward
What you bring
- A bachelor’s degree in a scientific or healthcare-related field
- A track record managing clinical research science, including project coordination and data analysis
- Experience leading cross-functional teams and handling complex projects with strong organization and leadership
- Knowledge of research methods, study design, and regulatory requirements, plus relevant analytical tools
Who this fits
This senior role suits someone who can lead scientific work across clinical research projects, manage competing priorities, and guide a team. You must have legal authorization to work in the country where the role is based.
From the employer
At 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 Scientific Manager at ICON, you will manage the scientific aspects of clinical research projects, ensuring the highest standards of scientific excellence and operational efficiency.
What You Will Do:
You will oversee scientific operations workstreams, ensuring deliverables meet quality and timeline expectations.
Key responsibilities include:
- Managing the scientific and operational aspects of clinical research projects, ensuring adherence to protocols and timelines.
- Collaborating with cross-functional teams to develop and implement research strategies and solve complex scientific challenges.
- Overseeing the design, execution, and analysis of study protocols, ensuring high-quality data collection and interpretation.
- Providing guidance and support on scientific methodologies, data analysis, and regulatory compliance throughout the project lifecycle.
- Building and maintaining relationships with stakeholders, including research partners and regulatory agencies, to advance project goals and drive innovation.
Your Profile:
You will have solid scientific operations experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Proven experience in managing scientific aspects of clinical research, with a strong focus on project management and data analysis.
- Strong leadership and organizational skills, with experience in leading cross-functional teams and managing complex projects.
- Expertise in scientific methodologies, study design, and regulatory requirements, with proficiency in relevant analytical tools.
- Excellent communication and interpersonal skills, with the ability to influence stakeholders and ensure successful project outcomes.
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
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