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senior medical writer
The Senior Medical Writer will be responsible for working across several accounts and therapy areas. They will provide scientific input into the project strategy and develop engaging and accurate copy for selected healthcare communications projects covering scientific communications, brand communications and patient communications. These can range across a wide variety of media including, but not limited to, digital applications, web-based projects, print materials, internal communications, storyboards, slide decks and meeting materials.
The Senior Medical Writer will also be responsible for supporting junior members of the team, either through coaching or review of their work and providing constructive criticism. Finally, the senior medical writer will participate in proposals and pitches for their accounts and/or potential new clients in their key therapy areas.
Previous roles/experience would include:Medical Writer
Usually reports into:Scientific Director or Editorial Team Lead
Sits within this team:Editorial or Medical Writing
Qualifications:PhD Minimum
Salary band:£35,000 - £50,000 Basic Salary, Pension, Annual Leave, Gym membership, Cycle to work scheme
Related topics:Senior Medical Writer, Medical Communications, Healthcare Communications, MedComms, Medical Education, Medical Writing, Homeworking, Pharmaceuticals, Publications, Editorial, PhD, Communications, Science Writing
Senior Medical Writer jobs
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Global Medical Affairs Director - Vaccines
Permanent / Berkshire, England
Global Medical Affairs Director - Vaccines Pharma-Partners is currently recruiting a Global Medical Affairs Director for a leading vaccines specialist, pharmaceutical company This opportunity will be a highly visible and influential role within the organisation working with multiple cross functional groups to deliver on projects and implement strategy. It provides a great opportunity to utilise your expertise in the vaccines field when communicating with external experts and internal stakeholders. Responsibilities: Responsible for developing and executing strong strategic medical plans for products, providing decision-makers around the world with the evidence and confidence they need to scientifically differentiate our vaccines, in alignment with seasonal portfolio. Accountable for all global medical activities in the portfolio, including leading development and implementation of global medical strategy, aligning with company strategies, and communicating with regional and country medical leads. Participate in nominated Medical Affairs and Cross-Functional Project Teams Interface with the scientific community either through direct/virtual interaction and establish relevant relationships with government officials and external experts as appropriate. Provide medical insight, scientific expertise and medical leadership to the team and participate in key strategic decisions that impact the life cycle planning of products The Candidate: Advanced Degree of MD, PharmD or PhD in a scientific discipline is preferred Previous Medical Affairs experience required, ideally at a global or regional level Relevant therapeutic experience within vaccines or infectious diseases Strategic mindset, strong influencer and great communication skills Remuneration: Basic annual salary depending on experience plus a standard benefits package To apply for this position please use the "Apply" option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk
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Medical Science Liaison - North UK
Permanent / Manchester, Greater Manchester
Medical Science Liaison - North UK Pharma-Partners is currently supporting a specialist global pharma company with a new MSL team build in preparation for a key product launch. This role will be a key part of a growing medical affairs team. Not only would this position be key in external interactions with KOLs and HCPs across the UK but will have insights and input into medical plans and wider business activities, supporting the Medical Managers and Medical Director where required. Responsibilities: Develop and maintain long-term professional relationships with clinical trial investigators, key opinion leaders (KOLs) and HCPs Utilises superior therapy area and product knowledge to engage with HCPs through non-promotional evidence-based scientific dialogue and presentations Discuss scientific research concepts and ideas with investigators Provide/develop speaker training to ensure scientific and medical accuracy Collaborate with colleagues to actively support medical and scientific meetings by collecting and interpreting insights competitive intelligence /presentations/ results The Candidate: Advanced Degree of PharmD, MD or PhD in a scientific discipline is preferred Previous Medical Science Liaison Experience, ideally in a pre-launch setting Relevant therapeutic experience within immunology/rheumatology/nephrology Strategic mindset, strong influencer and great communications Remuneration: Basic annual salary depending on experience plus a standard benefits package To apply for this position please use the "Apply" option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk
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Medical Science Liaison (MSL) - Oncology - North UK
Permanent / West Yorkshire, England
Medical Science Liaison (MSL) - Oncology - North UK Pharma-Partners is working with a small/mid-sized speciality pharma company with expertise in Oncology. Our client is recruiting a Medical Science Liaison to join their field based Medical Affairs team and cover the North UK. As an MSL you will be expected to build partnerships and engage with Healthcare Professionals (HCPs) across the designated territory in the communication evidence based scientific insights. You will work across the Oncology portfolio. Key responsibilities: Establish and maintain relationships with Oncology experts across the region Provide scientific expertise and technical support to Key Opinion Leaders (KOLs) Deliver therapeutically aligned scientific presentations to HCPs Provide medical support as part of a cross functional team to relevant clinical development studies Focussing on patient outcomes, develop local guidelines to support the use of the company's Oncology products Ensure adherence to company SOPs and medial compliance Work with office-based colleagues in Medical and Brand teams, as well as other field-based colleagues, to provide scientific support and education for the company's products Candidate Requirements: Educated to higher degree level (MD, MPharm, PhD, MSc) Experience in the UK pharmaceutical industry is essential Therapeutic area expertise in Oncology Experience in external engagement or customer facing roles Effectively assimilate scientific and clinical data to the relevant audience Understanding of the UK healthcare space Salary & Remuneration: Competitive basic annual salary plus a benefits package to include company car and annual bonus To apply for this position please use the "Easy Apply" option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk
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Global Medical Affairs Director - Vaccines (East Coast US)
Permanent / New Jersey, USA
Global Medical Affairs Director - Vaccines Location: East Coast, USA Pharma-Partners is currently recruiting a Global Medical Affairs Director for a leading vaccines specialist, pharmaceutical company This opportunity will be a highly visible and influential role within the organisation working with multiple cross functional groups to deliver on projects and implement strategy. It provides a great opportunity to utilise your expertise in the vaccines field when communicating with external experts and internal stakeholders. Responsibilities: Responsible for developing and executing strong strategic medical plans for products, providing decision-makers around the world with the evidence and confidence they need to scientifically differentiate our vaccines, in alignment with seasonal portfolio. Accountable for all global medical activities in the portfolio, including leading development and implementation of global medical strategy, aligning with company strategies, and communicating with regional and country medical leads. Participate in nominated Medical Affairs and Cross-Functional Project Teams Interface with the scientific community either through direct/virtual interaction and establish relevant relationships with government officials and external experts as appropriate. Provide medical insight, scientific expertise and medical leadership to the team and participate in key strategic decisions that impact the life cycle planning of products The Candidate: Advanced Degree of MD, PharmD or PhD in a scientific discipline is preferred Previous Medical Affairs experience required, ideally at a global or regional level Relevant therapeutic experience within vaccines or infectious diseases Strategic mindset, strong influencer and great communication skills Remuneration: Basic annual salary depending on experience plus a standard benefits package To apply for this position please use the "Apply" option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk
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Regulatory Affairs Senior Associate, Global Publishing
Permanent / Oxfordshire, England
Job title: Regulatory Affairs Senior Associate, Global Publishing A Biopharmaceutical company in Oxfordshire are seeking a Senior Associate, Global Publishing to join their Regulatory Operations team. This role will be responsible for the preparation and publishing of documentation for commercial and development submissions to global health authorities. Responsibilities: Support Regulatory Affairs team in planning, publishing, submission, and archive of regulatory documents. Prepare and publish regulatory submissions in eCTD format, including, but not limited to: amendments; supplements; periodic/annual reports; promotional materials and meeting packages. Work across company disciplines and represent Global Regulatory Operations on assigned project and/or task teams to effectively communicate and drive timings and deliverables. Maintain records in Regulatory Information Management (RIM) system. Requirements: Direct experience with publishing, compiling, preparing and QC of documents for eCTD submissions. Demonstrates a working knowledge of Regulatory Information Management system and publishing technologies. Experience with Global Submit Review/Publish, ISIToolBox, Starting Point templates, and Veeva Vault a plus. 3+ years of Regulatory Operations experience preferred. Salary and benefits: A competitive salary, annual bonus and wider benefits package is on offer with this role. To apply for this position or hear further details then please contact Matt Thomas via matt.thomas@pharma-partners.co.uk
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