Remote, UK time zone as you will be working with the UK market.
About Greenpark
Greenpark is a global, award-winning, performance-driven content leader and brand publishing agency. Our Purpose is to help brands create meaningful connections that impact people’s lives through performance-driven content for search and social. Our unique expertise in Omnichannel Search & Insights, Creative Content and Performance Tech are delivered to our clients via an ad agency and in-house model.
We do this for a global client portfolio including Unilever, Campari Group, AIA, Sanofi, Nestle, Lipton, Kimberley Clark, Straumann, Ricola, Globe Telecom, and more.
Our Values
As a company, we strive and act together in our ambition to make a positive impact for the people and brands we serve, we do everything with kindness and respect at the core. ‘We Strive’, ‘Acting Together’, ‘With Kindness’ are the values that guide us.
About the role
As an Junior Medical Content Editor you will have an important role in providing support to the Content team. You will be required to immerse yourself in the Online/Digital media world, learning quickly and honing your skills and knowledge of the industry.
Your role will be crucial in assisting the Content team, providing support in creating reference packs, and in working on assignments.
About you
- Ensure compliance to local legislation and regulations including our client’s UK internal policies, ensuring that content is reference tagged properly
- Good understanding of our client’s UK oncology brands and can help with quicker turnaround for reference tagging tasks
- Should have strong understanding of the complete MLR (Medical, Legal, Regulatory) approval process
- Work in partnership with the graphic design team (on the amends for copy and content), with the brand and production teams and project deliveries.
- Should be able to create reference packs on Veeva Vault based on the brief shared across by the brand team
- Should be able to suggest from where we can source the appropriate references for different assets
- Should be able to mark-up PDFs in the case of re-ordering of citations and work closely with the design and production team to explain them the same
- Follow best practices in the department regarding processes, communication (internal and external), project management, documentation and technical requirements
- Participate in assigned training programs and work on assignments as per requirement
- Being compliant to quality, confidentiality, and security; adhering to and following quality systems, processes, and policies; and being compliant to training and specifications
- Education—B Pharm/M Pharm/BDS/MDS/PhD
- Minimum 3 years of experience in an agency setting
- Strong flair and passion to work for the pharmaceutical market
- Passion for networking and stakeholder engagement.
- Being up-to-date with the latest technical/scientific developments and relating them to various projects
- Client-oriented attitude with focus on creating strong long-term relationships with clients and encouraging others to work toward this goal
- Ability to assure timely completion of assignments
- Skilled in problem identification and problem solving
- Detail oriented, well organized and timeline driven with the ability to multitask.
- Experience working within a big multi-national company in a matrix environment.
- You live & breathe Greenpark’s core values—championing openness, respect, innovation, and teamwork—so that every interaction, both internally and externally, reflects our commitment to our values.
At Greenpark, we believe the best ideas come from the widest range of perspectives. We welcome and celebrate every background, identity, and experience across our global workforce. By fostering a culture of respect, inclusivity, and collaboration, we’re committed to ensuring everyone’s voice is heard and everyone can thrive.
All applications shall be considered for employment without regard to race, ethnicity, religion, gender, sexual orientation, gender identity, age, neurodivergence, disability status or any other protected characteristics.