Piedmont Healthcare

Informed Consent Writer

US, Blue Bell (ICON) · Contract

Sponsorship not specifiedDetected 8 days ago

Data AnalysisStatisticsAccessibilityExcelClinical TrialsClinical ResearchResearchCommunicationCollaborationOrganizational SkillsMicrosoft Office

About the role

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Inclusion and Accessibility ICON is an equal opportunity employer.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Conducting literature reviews, data analysis, and interpretation of clinical trial results to support the development of scientific manuscripts, abstracts, posters
Participating in project meetings, teleconferences, and client interactions to discuss project objectives, timelines, and deliverables, while providing input and feedback on document content, format, and presentation.
Strong attention to detail and organizational skills, with the ability to manage multiple tasks simultaneously, prioritize workload effectively, and meet project deadlines in a fast-paced environment.
We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with document management systems, reference management software, and statistical analysis tools preferred.

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
Visit our careers site to read more about the benefits ICON offers.
Your role will involve delivering medical writing work to a high standard, working closely with your team and stakeholders.
You will bring relevant medical writing experience, along with the following qualifications and skills.
Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field, with a keen interest in medical writing, clinical research, and drug development processes.
Excellent written and verbal communication skills, with the ability to translate complex medical and scientific information into clear, concise, and engaging content tailored to diverse audiences.
Motivated self-starter with a passion for learning and professional growth, committed to delivering high-quality work and contributing to the success of clinical research initiatives.
Rewards & Benefits

Informed Consent Writer
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 Medical Writer I at ICON, you will the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of innovative treatments and therapies.
Demonstrated ability to work collaboratively as part of a multidisciplinary team, communicate effectively across different functional areas, and adapt to changing project requirements and priorities.

This listing is sourced directly from Piedmont Healthcare's careers page and normalized into a canonical job model.