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summary

hong kong
randstad hong kong
permanent
full-time

specialism
life sciences
sub specialism
clinical & technical support
reference number
91M0205605_5410214138159495839

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job details

about the company.

Our client, a world-class leading pharmaceutical manufacturing company, is currently looking for an enthusiastic Site Start-up Manager to join their expanding team.

...

about the job.

Collaborate with SSO Study Start-Up Team Lead, SSO Country Head Portfolio/SSO Cluster Head Portfolio to support country SSU strategy and ensure SSU timelines and deliverables are met
Accountable for timely start-up activities from country allocation until Green Light in assigned projects, including preparation of IRB/IEC submission packages, review of Informed Consent Forms, and engaging Regulatory Affairs/CTA Hub for Health Authorities submissions
Prepare and finalize local submission packages for submission to IRB/IEC, CTA Hub, and Health Authorities as applicable, and coordinate timely response to deficiency letters and reportable events
Ensure timelines, accuracy, and quality of country TMF documents in study start-up to ensure TMF inspection readiness
Support study feasibility and lead site selection in collaboration with Feasibility Manager and Site Partnership Manager and the global study team
Ensure sites are prepared for "Green Light" and oversee local SSU team activities in assigned studies to achieve start-up timelines and quality execution.
Lead/chair local SSU team meetings and participate in global study team meetings as required
Lead the development of country site initiation and patient enrollment plans together with SSU CRA, CPM, and SSU Lead

skills & experiences required.

Degree in scientific or health discipline required, advanced degree with clinical trial experience and/or project management is preferable
Minimum 5 years' experience in clinical operations overseeing and/or monitoring clinical trials
Capable of leading in a matrix environment without direct reports
Understanding of all aspects of clinical drug development, particularly trial set-up, execution, and monitoring
Strong project management capabilities with demonstrated ability to problem-solve and mediate complex issues
Thorough understanding of international drug development processes, including knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/national health authority regulations, and Novartis standards
Strong interpersonal, negotiation, and conflict resolution skills
Effective communication in a local/global matrixed environment
Fluent in both written and spoken English, local language as needed

Interested individuals can click apply now and send through an updated resume in WORD format. For a more comprehensive list of current opportunities, please visit https://www.randstad.com/jobs/q-hong-kong/ or contact Jessica Cheung at + 852 6285 6991 or email jessica.cheung@randstad.com.hk

#humanforward

about the company.

Our client, a world-class leading pharmaceutical manufacturing company, is currently looking for an enthusiastic Site Start-up Manager to join their expanding team.

...

about the job.

Collaborate with SSO Study Start-Up Team Lead, SSO Country Head Portfolio/SSO Cluster Head Portfolio to support country SSU strategy and ensure SSU timelines and deliverables are met
Accountable for timely start-up activities from country allocation until Green Light in assigned projects, including preparation of IRB/IEC submission packages, review of Informed Consent Forms, and engaging Regulatory Affairs/CTA Hub for Health Authorities submissions
Prepare and finalize local submission packages for submission to IRB/IEC, CTA Hub, and Health Authorities as applicable, and coordinate timely response to deficiency letters and reportable events
Ensure timelines, accuracy, and quality of country TMF documents in study start-up to ensure TMF inspection readiness
Support study feasibility and lead site selection in collaboration with Feasibility Manager and Site Partnership Manager and the global study team
Ensure sites are prepared for "Green Light" and oversee local SSU team activities in assigned studies to achieve start-up timelines and quality execution.
Lead/chair local SSU team meetings and participate in global study team meetings as required
Lead the development of country site initiation and patient enrollment plans together with SSU CRA, CPM, and SSU Lead

skills & experiences required.

Degree in scientific or health discipline required, advanced degree with clinical trial experience and/or project management is preferable
Minimum 5 years' experience in clinical operations overseeing and/or monitoring clinical trials
Capable of leading in a matrix environment without direct reports
Understanding of all aspects of clinical drug development, particularly trial set-up, execution, and monitoring
Strong project management capabilities with demonstrated ability to problem-solve and mediate complex issues
Thorough understanding of international drug development processes, including knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/national health authority regulations, and Novartis standards
Strong interpersonal, negotiation, and conflict resolution skills
Effective communication in a local/global matrixed environment
Fluent in both written and spoken English, local language as needed

Interested individuals can click apply now and send through an updated resume in WORD format. For a more comprehensive list of current opportunities, please visit https://www.randstad.com/jobs/q-hong-kong/ or contact Jessica Cheung at + 852 6285 6991 or email jessica.cheung@randstad.com.hk

#humanforward

skills
no additional skills required
qualifications
no additional qualifications required
education
Bachelor Degree

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jessica cheung

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site start-up manager, sso.

job details

about the company.

Our client, a world-class leading pharmaceutical manufacturing company, is currently looking for an enthusiastic Site Start-up Manager to join their expanding team.

...

skills & experiences required.

Interested individuals can click apply now and send through an updated resume in WORD format. For a more comprehensive list of current opportunities, please visit https://www.randstad.com/jobs/q-hong-kong/ or contact Jessica Cheung at + 852 6285 6991 or email jessica.cheung@randstad.com.hk

#humanforward

about the company.

Our client, a world-class leading pharmaceutical manufacturing company, is currently looking for an enthusiastic Site Start-up Manager to join their expanding team.

...

skills & experiences required.

Interested individuals can click apply now and send through an updated resume in WORD format. For a more comprehensive list of current opportunities, please visit https://www.randstad.com/jobs/q-hong-kong/ or contact Jessica Cheung at + 852 6285 6991 or email jessica.cheung@randstad.com.hk

#humanforward

skills

qualifications

education

the application process.

apply with randstad.

we’ll give you a call.

getting you registered.

compliance check.

reference and background check.

the perfect job for you.

the interview.

start your new job.

get in touch

jessica cheung

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regional product manager (apac) (med device)

territory manager - orthopedics - medical devices

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