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Clinical Medical Manager

3+ years
Not Disclosed
10 Nov. 22, 2024
Job Description
Job Type: Full Time Education: MBBS/MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About Novo Nordisk

Novo Nordisk is a global healthcare leader with over 100 years of expertise in combating serious chronic diseases. Our commitment to improving the lives of millions of patients worldwide has established us as one of the top 20 most valuable companies in the world by market cap. We are expanding our reach, making a difference in the lives of over 40 million patients daily. Join us to contribute to a life-changing mission focused on collaboration, innovation, and transforming healthcare.


Department Overview: CMR (Clinical, Medical, Regulatory & Pharmacovigilance)

The CMR team is dedicated to driving clinical trials and providing medical/scientific expertise in New Therapy Areas such as CVD (Cardiovascular Disease), CKD (Chronic Kidney Disease), and NASH (Non-Alcoholic Steatohepatitis). Based in Delhi, we work closely with KOLs (Key Opinion Leaders), investigators, and patient advocacy associations to ensure the successful execution of clinical trials with a strong focus on scientific excellence and patient outcomes. The atmosphere within the team is collaborative, dynamic, and centered on achieving clinical research success.


Position: Clinical Medical Manager

Location: Delhi
Department: CMR (Clinical, Medical, Regulatory & Pharmacovigilance)

As a Clinical Medical Manager at Novo Nordisk, you will be responsible for providing medical and scientific expertise to support the execution of clinical trials in new therapy areas, including CVD, CKD, and NASH. You will engage with key external stakeholders such as KOLs, investigators, and research centres to ensure successful trial outcomes.

Key Responsibilities

  • Clinical Trials Execution:

    • Facilitate the execution of clinical trials across Phase I-IV in new therapy areas, including CVD, CKD, and NASH, by providing medical/scientific advice.
  • KOL and Investigator Engagement:

    • Identify and map Key Opinion Leaders (KOLs), investigators, and relevant research centres within the assigned therapy areas.
  • Scientific Insights & Communication:

    • Collect early scientific insights and provide guidance by engaging in discussions with external experts about early development data.
    • Contribute to scientific communication internally and externally, requiring strong presentation skills.
  • Clinical Support & Training:

    • Provide medical guidance and internal training to clinical staff to ensure proper understanding of trial protocols and methodologies.
  • Site Visits & Investigator Meetings:

    • Perform ad hoc site visits, attend investigator meetings, and ensure KOL inclusion in clinical trials.
    • Engage key investigators to communicate trial results and ensure successful trial participation.

Qualifications

We are looking for candidates who meet the following criteria:

  • Education:

    • MBBS/MD with a strong background in clinical research or medical affairs.
  • Experience:

    • 3+ years of experience in the clinical or pharmaceutical industry, with hands-on experience in human healthcare research, either from universities, CROs, or the pharmaceutical industry.
    • Expertise in relevant therapeutic areas (CVD, CKD, NASH), with a preference for candidates with authorship in peer-reviewed journals.
    • Experience as a clinical trial investigator or sub-investigator is a plus.
  • Skills & Competencies:

    • Strong understanding of pharmaceutical drug development and clinical trial processes.
    • Willingness to travel domestically and internationally for site visits, congresses, and company events.
    • In-depth knowledge of the local healthcare infrastructure and its specificities.

Working at Novo Nordisk

At Novo Nordisk, we strive for more than just success – we aim to create life-changing outcomes for patients globally. With over 63,000 employees worldwide, we collaborate across borders to transform healthcare. By joining our team, you will be part of a collective effort working toward innovative solutions for chronic diseases and making a lasting impact on patients' lives.


Application Process

To apply, please submit your CV and motivational letter through our online application tool.

Deadline: 30th November 2024


Important Disclaimer

Beware of fraudulent job offers that may pose as Novo Nordisk recruiters. Novo Nordisk never extends unsolicited job offers or asks for personal information or payments for recruitment purposes. If you receive any suspicious offers, please verify them through our official channels.


Commitment to Diversity and Inclusion

At Novo Nordisk, we are committed to building an inclusive culture that values and celebrates diversity. We believe that the unique perspectives of our employees enable us to create a stronger, more innovative company. Our commitment to equality ensures that all job applicants have an equal opportunity to succeed. Together, we’re life-changing.