Clinical Study Manager

Quanta Consultancy Services Ltd; United States; Remote; USD 60,000 - 80,000; Full time

Job summary

An exciting opportunity awaits you as a Clinical Study Manager with a focus on impactful clinical trials. Join a forward-thinking company dedicated to advancing patient care through innovative research and product development. In this role, you will advocate for patients, ensuring their needs are met while managing clinical projects effectively. Your expertise in clinical project management and vendor coordination will be crucial as you work alongside talented teams to drive the success of life-changing studies. If you are passionate about making a difference in the lives of patients and thrive in a collaborative environment, this position is perfect for you.

Qualifications

• Bachelor's degree with clinical research experience and 2+ years in project management.
• Experience in managing clinical teams and external vendors.

Responsibilities

• Act as a patient advocate throughout the clinical development project lifecycle.
• Coordinate with Medical and Quality Assurance to identify risks to clinical trial projects.

Skills

Clinical Project Management

Patient Advocacy

Vendor Management

Cross-functional Team Liaison

Fluency in Chinese

Education

Bachelor's Degree in Clinical Research

Job description

Clinical Study Manager – Australia - Contract

We have an exciting opportunity with an Australian based client who’s focus on the research, development, and commercialisation of products helps patients who haven’t yet received necessary care. You would contribute to their portfolio of life changing products as a Clinical Study Manager in their newest facilities.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:

• Act as a patient advocate throughout the clinical development project lifecycle, with a mindset to minimize patient and site burden when participating in clinical trials.
• Understand and support trial milestones including site identification and assessment, patient/subject recruitment, Key Opinion Leader (KOL) and Steering Committee development, and medical affairs support as required.
• Coordinate internally with Medical and Quality Assurance to identify risks to clinical trial projects.
• Participates in the development of study timelines, in coordination with the internal study team and external partners. Manages the trial according to agreed timelines.

Desirable Experience:

• Bachelors with experience in clinical research, with at least two years of clinical project/study management.
• Experience qualifying & managing external vendors (e.g. CRO, Call Center, Central labs, etc.).
• Experience managing clinical project team personnel.
• Experience leading operational teams through the start-up, study conduct, data management, and report writing of clinical studies.
• Experience liaising cross-functional teams internally and with external partners to align on program expectations.
• Fluent in Chinese

If this role is of interest to you, please apply now!




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