Medical Writer - South Africa at ApotheCom

Durban, KwaZulu-Natal, South Africa -

Full Time

Start Date

Immediate

Expiry Date

09 Feb, 26

Salary

0.0

Posted On

11 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Excellent Written And Verbal Communication Skills, Scientific Writing And Editing Ability, Experience Of Writing Scientific Publications, Project Management Skills, Organisational Skills, Flexibility, Adaptability, Resourcefulness, Time Management Skills, Judgment And Problem-Solving, Quality Control Skills, Attention To Detail, Client-Centric Attitude, Ability To Work Independently, Teamwork, Understanding Of Pharmaceutical Issues

Industry

Pharmaceutical Manufacturing

Description

Inizio Medical has built a large team of medical writers in South Africa, becoming the leading medical communications company in Africa. We are recruiting for a new intake of medical writers who will start with us in March 2026. Our teams in South Africa work alongside our global teams (based in the US, UK, South Africa and EU) in our three med comms agencies: ApotheCom, Nucleus Global and Ashfield MedComms. This will give you the opportunity to work on cutting edge science with world-leading experts in a variety of therapy areas, and help to deliver impactful results for the healthcare community. To give you the best start in your med comms career, you will receive industry-leading, award-winning training through our allegro.WRITE training programme. During your first six weeks with the company, a dedicated team of experts will provide training and individual mentoring focussed on developing writing skills, project management, teamwork and networking, allowing you to build confidence and ability. Combining complex scientific understanding with creativity, Inizio Medical develops impactful medical affairs strategies and compelling communications. Underpinned by world-class medical analytics capabilities and applied AI tools, Inizio Medical redefines the role of medical affairs in drug development and commercialization. Principal Role: You are responsible for (a) researching and developing technical medical material, (b) ensuring that all outputs adhere to the written brief, are accurate in content and editorial style and can be referenced, (c) liaising with clients and medical experts on content development, (d) attending scientific and client meetings where output is required. Academic Background: An advanced degree in a biomedical subject Skills Required: Excellent written and verbal communication skills Demonstrate excellent and versatile scientific writing and editing ability Experience of writing scientific publications and conference presentations Ability to generate materials to a high standard and quality, with minimal internal review/assistance Excellent project-management and organisational skills Flexibility, adaptability and resourcefulness Good time management skills Judgment and problem-solving Excellent quality control skills and meticulous eye for detail – style/consistency, grammar, scientific accuracy, proof-reading, layout, etc. Ability to ensure all writing meets the client’s strategic marketing objectives, as well as being of high scientific quality/credibility Understanding of pharmaceutical and health-related issues Strong sense of responsibility and urgency; ability to take ownership of projects Ability to work independently under limited supervision Solid understanding of human pathophysiology and disease; ability to learn new and diverse subject areas quickly Ability to work within a team and form productive working relationships within, and external to, Huntsworth Health Strong client-centric attitude - ability to work with clients on projects, ensuring they meet strategic marketing and medical needs Flexibility and ability to manage simultaneous priorities, changing deadlines, and limited resources. IT skills – Word, PowerPoint, internet searching We encourage all candidates who meet the minimum criteria of this role, to apply for this role. We confirm that we are a designated employer and as such where reasonable, possible and/or appropriate we will give priority to the goals set out in our employment equity plan. The company will provide all the necessary equipment to perform the role (including laptop, headset, keyboard, mouse and stipend towards data package. Inclusivity is key to us, if you require any reasonable adjustments due to disabilities or other needs during the recruitment process, please inform us. Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.

Responsibilities

You will be responsible for researching and developing technical medical material while ensuring accuracy and adherence to editorial style. Additionally, you will liaise with clients and medical experts on content development and attend scientific and client meetings.