Job Description

About the jobDepartment Clinical Reporting UnitDoes your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career objectives? Then we might have the right position for you. Apply now and join a growing team, working in an international environment.About The DepartmentThe Clinical Reporting unit in GBS has seen a tremendous growth curve and has become an integral part of the Global Clinical Reporting community in a short span of 6-7 years, since its inception in 2011. The team is a dynamic mix of enthusiastic and qualified skilled Medical Writers, Disclosure Associate Medical Writers, Publishers, and Document Controllers with master/PhD in life sciences, pharmacology, medicine, etc. The team is full of commitment, passion, skills, and talent with broad knowledge of different therapeutic areas and regulatory requirements for submissions. The team has an average experience of 7-8 years in writing and reviewing regulatory documents and publications. We use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials. Apart from writing and publishing regulatory documents, the team is also responsible for the distribution of documents (CONNECT portal) and largely contributes to NNs regulatory commitments by being involved in Public disclosure activities.The PositionAs an Associate Medical Writer, you will ensure timely, clear, and proactive communication and collaboration with the stakeholders and colleagues globally. Furthermore, you will communicate across the time zones and in different professional environments. This job requires good communication and analytical skills. To meet timelines, you must be good at planning your work be proactive when problems arise, and seek help and advice from relevant people within GBS as well as within Head Quarters (HQ). Additionally, you will challenge the expert contributors on the clinical documents where the quality of their written contribution could be improved. You are entrusted to fulfill the following responsibilities:Ensure timely, clear, and proactive communication and collaboration with the stakeholders and colleagues globally.You will contribute to process improvements, knowledge sharing, and skill building, and mentor and train other Associate Medical Writers as needed. You will have to maintain good relationships with the stakeholders and colleagues.Responsible for meeting timelines, the Associate Medical Writer must be good at planning their work be proactive when problems arise, and seek help and advice from relevant people within GBS as well as within HQ.You will challenge the expert contributors on the clinical documents where the quality of their written contribution could be improved.QualificationYou are expected to have the following skills and knowledge:Graduate (PhD, MSc., M Pharm, or equivalent).2+ years of experience as an Associate Medical Writer or other relevant work experience.Experience working within a global setting.Experience in the pharmaceutical /CRO industry.Strong understanding of external requirements related to regulatory documents.Good communication skills.Works independently on smaller tasks.Strong analytical skills.Committed, persistent, and accountable.Able to plan and manage variable workload.Working at Novo NordiskNovo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we\'re working toward something bigger than ourselves, and it\'s a collective effort. Join us! Together, we go further. Together, we\'re life-changing.Lifelancer ( ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.Please use the below Lifelancer link for job application and quicker response.

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