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Our Company Culture

Be part of our forward-thinking team and experience a pleasant work environment.

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Passionate Approach

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    Professional Development We are committed to the professional growth and development of our employees. We offer a supportive and stimulating environment that encourages continuous learning, provides access to industry-leading resources, and offers opportunities for career advancement.
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    Global Network Joining HiRO means becoming part of a vast global network of biotech professionals, research institutions, and industry partners. This network opens doors to exciting collaborations, knowledge sharing, and exposure to diverse perspectives, enriching your professional journey.
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    Collaboration and Innovation At HiRO, collaboration and innovation are at the core of our work culture. You'll have the chance to collaborate with renowned researchers, key opinion leaders, and industry experts, fostering creativity and driving breakthrough solutions.
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CRA II / Sr CRA ClinOps

Department: Clinical Operations

Years: 2+ years (CRA II); 5+ years (Sr. CRA)

Education: Bachelor’s Degree

Qualification/Criteria 

Bachelor’s degree in Life Sciences or an equivalent combination of education, training, and experience. Certified Healthcare Professionals (e.g., Registered Nurse, Licensed Practical Nurse, MD, etc.) are strongly preferred.
Demonstrated on-site monitoring experience.
For CRA II, 2+ years of experience is required.
For Sr. CRA, 5+ years of experience is required.
Excellent oral and written communication skills in English, including proficient presentation skills.
Excellent communication, collaboration, and problem-solving skills.
Ability to travel.

Apply for this position: CRA II / Sr CRA ClinOps

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    Quality Manager

    Department: Experienced Recruitment

    Years: 5 -10 years

    Education: Regular College

    Duration: Full time

    Hiring: 1 person

    Qualification/Criteria 

    Bachelor’s Degree in Life Sciences or an equivalent combination of education, training & experience.
    Minimum of 5 years prior clinical industry experience (Clinical related experience such as PM, CRA, CTA is a plus)
    Extensive knowledge of GCP, ICH, 21 CFR part 11 guidance and strong organizational skills
    Previous experience of hosting/supporting inspection or audit is required
    Demonstrate ability to proactively and independently assess the compliance of clinical research activities per standards of GCP
    Capability of working in an international environment across regions, countries, and time zones.
    A good communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince and persuade. 
    Ability to travel as necessary (approximately 10%)
    Previous experience in people management is a plus
    Location: Shanghai or Beijing

    Apply for this position Quality Manager

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