Clinical Research Senior Manager

Amgen; United States; Remote; USD 120,000 - 180,000; Full time

Job summary

A leading biotechnology company is seeking a local development lead for phase I-III clinical development. The role focuses on developing novel drug molecules and requires a strong background in clinical research, particularly in oncology, inflammation, and rare diseases. The ideal candidate will have an MD degree and substantial experience in clinical trial design and execution.

Qualifications

• Minimum 5 years of clinical research experience in academia or biopharmaceutical industry.
• Experience in early and/or late-stage clinical trials and regulatory filings.
• Fluency in English and excellent communication skills.

Responsibilities

• Lead phase I-III clinical development strategy for Amgen pipelines in China.
• Contribute to study protocol and execution, ensuring GCP compliance.
• Collaborate with local/regional/global teams on clinical trials.

Skills

Clinical Research

Oncology

Inflammation

Rare Disease

Regulatory Knowledge

GCP Compliance

Statistical Analysis

Problem-Solving

Decision-Making

Cross-functional Team Collaboration

Education

MD degree from an accredited medical school

Job description

Career Category Clinical Development Job Description

We are building upon our long-term commitment to patients by developing a whole new class of novel molecules in oncology, general medicine, inflammation and rare disease – and we need top talent to ensure these molecules become medicines and realize their potential for helping patients.

Accountabilities

• To serve as local development lead for phase I-III clinical development of Amgen Pipelines
• To contribute to define, design, and execute clinical development as a strategy for drug development in China.
• To serve as key role in external collaboration and strategic partnership with key local sites in clinical studies and related research area
• To represent Medical Sciences internally and externally, contributing local medical insight into experimental design and data analysis.
• To provide subject matter expertise in clinical and translational trial science as well as the biology and treatment.

Responsibilities:

• Lead and/or contribute to designing, gaining approval of and executing high quality development strategy for assets in China, collaborating with cross-function local colleagues and global partners, together with key functional stakeholders and governance bodies
• Support the development and execution for clinical trials in China and be the local/regional medical science expert in resolving significant issues that may affect the studies
• Work closely with local/regional/global cross functional colleagues, including Clinical Operations, Patient Safety and Regulatory counterparts, to provide medical expertise to the study team
• Share local/regional clinical/scientific input during the development and execution of clinical trials
• In defined situations working under the Global Development Lead to :
• Contribute or lead development of and co-author clinical study protocol and related documents for example Key Design Elements (KDE), Clinical Study Reports (CSR), and clinical scientific publications (CSP).
• Serve as a member of the CST-LT, provide medical and strategic oversight to the study execution.
• Monitor, analyse, and interpret clinical study data
• Contribute to the preparation of documents required for regulatory submissions
• Develop and interface with local/regional industry key opinion leaders and manage scientific presentation at advisory boards, key scientific meetings and external committee meetings
• Participate in interactions with regulatory agencies
• Support the local/regional Brand Team in the brand planning process to ensure alignment between medical and brand activities, and help providing interpretation of clinical study data
• Ensuring compliance with GCP across clinical trials

Output

• Ensure local/regional/global clinical studies are adequately and timely supported and executed
• Ensure medical support leading to successfully submission and approval of CTNs and MAAs
• Establish and maintain appropriate relationship with local/regional industry key opinion leaders and medical communities

Skills and Qualities

• MD degree from an accredited medical school, and experience in patient care required
• Minimum 5 years of clinical research experience in academia and/or biopharmaceutical industry (biotech, pharmaceutical or CRO company)
• Demonstrate in-depth knowledge in the specific therapeutic areas of oncology, general medicine, inflammation or rare disease
• In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale
• Familiarity with concepts of clinical research and clinical trial design, including working knowledge of statistics as applied to clinical trial design and analysis
• Previous experience in early and/or late-stage clinical trials and regulatory filings
• Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication
• Experience in writing and editing scientific research reports
• Thorough understanding of GCP and familiarity with relevant NMPA and ICH guidance
• Ability to collaborate effectively in and/or lead cross-functional teams
• Strong commitment to goals and timelines
• Ability to absorb new information quickly and gain command of relevant literature
• Possessing excellent problem-solving & decision-making skills
• Excellent written and verbal communication skills, including fluency in English

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