Novo Nordisk

Clinical Medical Manager (Beijing, Beijing, CN)

Beijing, China Type not listed
Clinical Development Manager

Novo Nordisk is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Key responsibilities

Clinical Medical Managers deliver industry-leading clinical trial excellence and early therapy area development, with high-quality scientific insights and engagement, trusted partnerships, and innovation. They work in close partnership with Clinical Operations and Medical & Scientific Affairs to connect product development and world-class clinical trial execution with early therapy area development and successful product launches.

Main job tasks

1 Deliver industry-leading clinical trial excellence with scientific insights and external engagement

Partner with Clinical Operations Therapy Area Leads and Trial Managers on scientific and medical aspects of early trial planning, start up, recruitment and retention

Gather, analyse, communicate and implement actionable insights throughout the lifecycle of assigned clinical trials

Provide scientific inputs to trial portfolio review, country allocation and site feasibility processes

Lead ‘National Leader’ selection for relevant trials, and secure consideration for investigators who are important key opinion leaders during product launch for inclusion in the trials

Secure actionable scientific insights into protocol outline and trial execution to enhance outcomes

Contribute to site selection criteria, and assess medical capabilities as well as scientific training needs at sites

Engage relevant key opinion leaders who are investigators to optimise trial methodologies, mitigate recruitment and retention challenges, and build long-term relationships

Secure investigators and relevant site staff are well versed before FPFV with scientific aspects of the product, protocol, and measures to recruit and retain patients

Be the local subject matter expert on the product and protocol in relevant trials to discuss early clinical data with external experts during feasibility and to quickly resolve medical queries from site staff during the trial

Continuously monitor trial performance with Therapy Area Leads and Trial Managers and take proactive measures to address scientific issues (during retention Clinical Operations lead retention efforts and involve CMMs only if needed for scientific aspects)

2 Secure early inputs to product development, incorporating voice of patients and clinicians

Provide early medical and scientific input into product development, incorporating the perspectives of clinicians and patients

Identify and address potential challenges in product development through proactive scientific insights and stakeholder engagement.

3 Establish a strong presence in new and current therapy areas

Effectively communicate Novo Nordisk pipeline and scientific narrative to external stakeholders, especially those new to Novo Nordisk

Establish strong relationship with key stakeholders in new and current therapy areas through scientific engagement in trials

Secure mapping and updating of clinical care pathways for effective recruitment (including referrals) and retention in trials.

4 Build organizational readiness

In collaboration with Therapy Area Leads, co-design and deploy scientific knowledge building for Clinical Operations teammates on therapy area, product and protocol

Continuously exchange insights and introduce Medical Affairs colleagues to KOLs in new therapy areas, especially during pre-launch

5 Medical support to regulatory interaction

Medical input for clinical development strategy

Medical review and input for regulatory interactions and submissions

Other areas of responsibility

Be presenter at scientific conferences for oral presentation/poster based on NN sponsored trials

Be flexible to support projects as needed

Qualifications

MD, PhD, MSc, MPharm or equivalent in healthcare with strong background in clinical practice or research background

3+ years’ experience in clinical or medical roles in the pharmaceutical industry

Strong understanding of pharmaceutical drug development and value chain

Strong knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial methodology

An enterprise mindset demonstrating business understanding, prioritizing the organisation's overall success over own interests, and promoting cross-functional collaboration

Strong business acumen and understanding of business operations, financial drivers, and market dynamics

Excellent written and verbal communication, presentation skills and stakeholder management skills

Excellent ability to build and maintain strong relationships with internal and external stakeholders

Ability to creatively solve complex problems and drive the development of practical solutions.

Ability to innovate, identify opportunities for continuous improvement, and embrace change

Willingness to leverage technology such as AI tools and adopt a data-driven approach in all aspects of work

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

]]>

Job details

Seniority
Manager
Function
Clinical Development
Therapeutic area
Not listed
Location
Beijing, China
Employment type
Not listed

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 266 comparable Manager Clinical Development roles across 45 biopharma companies.

266Comparable roles tracked
230Currently active
45Companies hiring similar roles
29Countries represented

Salary context

64 of 266 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Clinical Trials Data Associate (P1) · Lilly $79,206/yr – $91,087/yr
Highest disclosed · Statistical Advisor · Gilead Sciences, Inc. $226,185/yr – $292,710/yr
Peer group range $85,146 – $259,448 (median $178,650)

Where these roles are based

Top locations among the 266 comparable roles

United States102
India50
China13
United Kingdom13
Poland13
Germany10

+ 23 more countries

Seniority mix

266 of 266 peers have a known seniority level

Manager145
Associate Director73
Associate48

Therapeutic area mix

26 of 266 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology9
Cardiovascular / CVRM6
Immunology6
Neuroscience3
Dermatology & Aesthetics1
Ophthalmology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
AbbVie Shanghai, Shanghai Manager
Same function Same seniority Same country
60%similar
Novartis Beijing (Beijing), China Manager
Same function Same seniority Same country
60%similar
Novartis Guangzhou (Guangdong Province), China Manager
Same function Same seniority Same country
60%similar
Boehringer Ingelheim Shanghai, China Manager
Same function Same seniority Same country
60%similar
Boehringer Ingelheim 上海, China Manager
Same function Same seniority Same country
60%similar
Boehringer Ingelheim Beijing, China Manager
Same function Same seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Clinical Supply Manager
AbbVie · Shanghai, Shanghai · Manager
Function Therapeutic area Seniority Country
60%
(Sr.)Clinical Trial Manager - CRM (Shanghai, China)
Boehringer Ingelheim · Shanghai, China · Manager
Function Therapeutic area Seniority Country
60%
(Sr.)Clinical Trial Manager - CRM (Shanghai, China)
Boehringer Ingelheim · Shanghai, China · Manager
Function Therapeutic area Seniority Country
50%
Clinical Research Associate II
BMS (China) Investment Co · Beijing, China · Associate
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.