上海招聘

Responsibilities:

- Supports activities related to development of the clinical data management systems (CDMS).

- Processes and reviews the CRF and external data.

- Supports and leads the clinical data review activities associated with a clinical trial.

- Prepares and completes quality control reviews and delivers the end product of an analyzable database.

- Serves as lead clinical data coordinator for one or more projects.

- Reviews clinical and external data for subjects enrolled in clinical research protocols based on edit specifications / data validation programs to facilitate data review.

- Maintains data management study documentation as appropriate.

- Performs proficient reviews of study datasets prior to client transfer.

- Manages the data review and external data reconciliation process.

- Mentors and trains other team members in data management skills and processes for individual studies.

- Utilizes internal systems to optimize and communicate resourcing issues and needs.

- Ensures study and task metrics are tracked and communicated to the project team and functional management.

- May participate in sponsor and/or third-party audits.

- Demonstrates strong knowledge of computerized information systems and standard application software (Windows, MS Office).

- Understands clinical data management systems or electronic data capture software.

- Exhibits strong knowledge of clinical data management.

- Displays excellent written and oral communication skills.

- Acts as a subject matter expert (SME) for various technologies or processes.

- Encounters problems that are varied but similar. Requires some fact-finding to define problem. Selects the best option from a set of defined procedures or based on precedence.

- Conveys or exchanges basic information in routine ways to audiences knowledgeable about the subject matter.

- Supports the achievement of goals through personal effort in own work area. Impact is limited to short-term achievement of goals.

Requirements:

- Work is typically performed in an office environment, using simple, easy muscular movements, involving only the handling of light materials, tools, or equipment in easy work positions, and with no special speed requirements or long stretches of exertion.

- Vision requirements for this job include close vision and the ability to adjust focus.

- Bachelor’s degree

- at least 1 years of clinical data experience

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!


For more information, please visit our website **************.