北京招聘

Our Study Start Up structure represents an integrated, dedicated, seamless team of experts, all striving to minimize cycle times. This is especially true of our dedicated and passionate Study Start Up Leads.

    

As a Start Up Lead, you will lead all aspects of Start Up activities at the regional level to achieve quick and successful activation of sites, overseeing and driving all aspects of study start up for your countries.   

    

Working through until last site activated, perform local EC submissions, prepare IP release packs and support sites at a local level. You will be working on a wide spectrum of projects in phase I-IV research at both GP practices and hospitals.

Responsibilities:

• Adopting our unique start-up methodology to drive early and predictable site activations through oversight of all activities, driving delivery and compliance across the assigned region
• Coordinate study start up activities, coaching and mentoring as appropriate
• Working collaboratively with functional colleagues and sponsors to ensure successful completion of study start up, fostering productive working relationships with other collaborators within Regulatory, Contracts and Clinical Team Management.
• Ensuring understanding and communication within each of your countries
• Eliminating all potential causes of delay
• Overseeing compliance and reporting progress.
• If assigned to a study as a Primary Start Up Lead, leading a monthly acceleration meeting and preparing reports for other internal stakeholders and the sponsor, coordinating a team of other Start Up Leads to ensure global success of study start up activities.

• To enable success in this position you will have:

1. A life-sciences undergraduate degree (or be a licensed healthcare professional)
2. A solid experience in managing study start up activities across a region, managing and meeting deliverables
3. A passion for study start up which drives you to motivate yourself and others
4. Previous experience of working in a CRO/pharma environment
5. An attitude that fosters collaboration and a sense of shared focus within a team

RPS Inc. is a next generation global CRO, headquartered in the United States with the operations in 45 countries throughout Americas (US, Canada, Latin America), EMEA and Asia Pacific regions. RPS provides comprehensive global Phase 1-4 clinical development solutions to the pharmaceutical, biotechnology and medical device industries. By combining an experienced clinical research operations infrastructure with the industry’s largest resourcing engines, RPS is uniquely positioned to offer our Clients both integrated and full service global outsourcing solutions. These solutions are powered by highly experienced and seasoned study teams providing innovative, cost-effective and high quality services.


RPS Asia Pacific Headquarters is located in Beijing, China and we have operations in 11 Countries in Asia Pacific region. With the rapid organic expansion of RPS in China & Asia Pacific, we are continuously looking for the experienced industry talents to join us.


Our specialized staff of consultants is eager to discuss your career plans. Tell us about yourself experience, so the appropriate consultant can contact you. RPS is sensitive to your daily responsibilities. Tell us EXACTLY how to contact you and we will. For your convenience, you can also submit your resume. We look forward to discussing the opportunities and benefits of employment with RPS!


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