Senior Manager, Clinical Scientist

🕒 June 24

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 39%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Gan & Lee Pharmaceuticals

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1998

🏥 Healthcare

🏭 Manufacturing

💊 Pharmaceuticals

💰 Private Equity Round - Gan & Lee Pharmaceutical on 2015-01

Healthcare • Manufacturing • Pharmaceuticals

Gan & Lee Pharmaceuticals is a China-based global pharmaceutical company focused on developing, manufacturing, and commercializing medicines and medical devices, with particular emphasis on diabetes and oncology treatments. The company conducts international clinical trials, registers and launches products across multiple regions, pursues licensing and partnerships for global rollout of drug candidates (for example, the GLP‑1 receptor agonist bofanglutide/GZR18), and promotes R&D, innovation, and corporate social responsibility.

📋 Description

• Provides scientific and/or medical expertise for clinical research aspects of the project • Participates in strategic meetings/advisory boards as key clinical research representative • Provides medical and scientific input to the core documents for the project (e.g., product strategy documents, target product profile (TPP), protocols, submission, etc.) • Consults with internal/external stakeholders and internal/external key opinion leaders • Provides support to other functional members of the project team • Interacts with investigators and CROs as the medical or scientific representative • Provides medical and scientific interpretation of efficacy and safety data • Participates in the interactions with regulatory authorities (e.g., FDA, EMEA meetings) • Provides input for a project publication plan, liaises with commercial and works on launch activities when required • Creates and reviews abstracts, and manuscripts created by internal or external sources

🎯 Requirements

• Medical Degree, PhD, or PharmD • At least 2-4 years in clinical development experiences at a pharmaceutical, biotechnology, CRO company, clinical training/practice, and/or academia • Experiences in metabolic diseases (Diabetes, Obesity, NASH, NAFLD, etc.), Endocrinology (CKD, CRF, etc.), and Nutrition and Weight Management related drug development are a plus • Board eligibility or certification preferred • Demonstrated ability to manage multiple and diverse projects concurrently • Demonstrated ability to develop positive relationships and collaborations • Strong analytical skills; a strategic thinker, planner, and implementer • Solid scientific skills and attentive to details • Working knowledge of biostatistics is a plus • Ability to operate independently with minimal supervision • Deep experience with literature analysis, proven technical English writing skills • Excellent written and oral communicator in English • Strong proficiency in major Microsoft Office products (i.e., Word, Excel, PowerPoint, Project)

🏖️ Benefits

• N/A