MakroCare is expert strategic development and commercialization global partner for pharmaceutical, biotechnology and medical device industries. Our experience, programs and processes bring a new dimension to development strategy, regulatory/risk planning & management, clinical research, medical/scientific support and emerging region expansion.

MakroCare has operations and presence in US, UK, EU, and Asia. MakroCare is well positioned to meet the demands of the expanding product portfolio needs of our life sciences clients worldwide. We also understand the demands of an increasingly competitive market.

Job Profile:

We are a Clinical Services Company currently seeking a freelance or contract Clinical Monitor for an exciting project with our medical device client in the Ophthalmology space.
Project Overview:

Frequency: 1 monitoring visit per month (2 days per visit).

Schedule: Highly flexible dates.

Duration: Estimated at 16 to 24 hours per visit.

Location : Shanghai

This role is fully flexible and structured on a freelance/consulting basis. We are prepared to offer a competitive, fixed price per visit based on your experience.

If this aligns with your current availability and interest, please share a few convenient times for a brief introductory call. When you reply, kindly include your standard hourly rate expectations in USD for reference.

If you are not available but know a qualified colleague who might be a good fit, please feel free to forward this opportunity to them.

Thank you, and looking forward to hearing from you.

Job Details:

Responsibilities:

Key Responsibilities:
• Manage daily clinical trial operations and ensure compliance with study protocols.
• Review clinical trial protocols and participate in the design and execution of clinical studies.
• Collaborate with clinical operations teams, providing support throughout the trial lifecycle.
• Conduct site monitoring as required, following instructions from the Project Manager (likely once or twice monthly).
• Perform data analysis, interpret results, and contribute to research efforts.
• Liaise with the medical and scientific community to provide necessary trial support.

Qualifications:

• Bachelor’s or Master’s degree in a related scientific field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• Strong knowledge and hands-on experience in clinical trials and monitoring.
• Proven ability to create, review, and implement clinical trial protocols.
• Experience in clinical operations, including site management, monitoring, and data management.
• Familiarity with Good Clinical Practice (GCP) and International Council for Harmonization (ICH) guidelines.
• Excellent communication, organizational, and analytical skills.
• Ability to work independently and remotely.

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