Senior/Regulatory Medical Writer

Hace 3 días

Barcelona, Barcelonés (comarca); Provincia de Barcelona; Cataluña, España Icon Clinical PLC Jornada completa

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Senior Medical Writer Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación.
- RemoteICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a global provider of drug development solutions, our work is serious business. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. As a Senior Medical Writer, your primary responsibility will be to provide scientific and medical/clinical writing support as part of a team dedicated to late-phase projects, servicing an assigned client. While the ability to work independently is key, the Senior Medical Writer will work closely with the ICON team and other members of the client account team to help ensure the timely delivery of high-quality and scientifically/medically accurate assigned projects.
The RoleThe primary responsibilities and accountabilities of our Senior Medical Writer are:Responsible for writing and reviewing study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report, etc.
Responsible for performing quality control for medical writing deliverablesResponsible for interpreting statistical results and for soliciting statistician input for developing study reports, abstracts, manuscripts, and other documents as requiredParticipating in the improvement of the quality assurance systemResponsible for participating in bid-defence presentations representing medical writing activitiesWhat you needAdvanced degree in a scientific discipline, preferably PhD, PharmD or MD5+ years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO or other health care settingProven knowledge of ICH/GCP and GPP guidelines or other meaningful guidelines or industry standardOutstanding written and verbal interpersonal skillsGood computer literacyAbility to work effectively and cooperatively with cross-functional teamsA strong desire to be a key part of a global network of services that lead to better outcomes for its clients, its people and for patients…apply now and Own #LI-SA1#LI-RemoteEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.
Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.
Ireland, DublinType: Full time

Senior/Regulatory Medical Writer

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