上海招聘

"At ICON, it's our People that set us Apart"

Clinical Data Project Manager

· Global Company

· Work / Life balance

· Great team environment

· Beijing Office-based

ABOUT DOCS:

DOCS - ICON Resourcing Solutions is a division of ICON plc that provides global staffing solutions to Pharmaceutical, Biotechnology, Medical Device companies and CROs in over 39 countries. We can recruit in virtually any location having access to offices in over 25 countries. This truly makes DOCS a company with global reach and personal focus. ICON has been in APAC since 1996 and the DOCS division of ICON is now expanding in the APAC region.

We are a specialist recruitment division / agency focusing in Clinical Research, Medical Affairs, Regulatory Affairs, Drug Safety, Health Economics, Data Management & Statistics, and Quality Assurance etc. Our full-spectrum resourcing solutions extend from contingent staffing, to functional resourcing, large-scale FSP and executive search. In addition, DOCS has developed a tailored training division "CRAcademy" to provide Traineeships and Training.

To learn more about DOCS, please go to www.docsglobal.com.

CURRENT VACANCIES:

Due to global growth, we are now recruiting for a Clinical Data Lead role for ICON. This role forms an integral part of an enthusiastic, inspirational, dynamic, friendly and supportive team.

Clinical Data Project Manager:

Beijing Office-based:

Role Responsibility

Responsible for managing data management teams, studies and programs of studies under the general direction of the Associate Dir/Dir of Data management.

Work with Clinical operations, Clinical Programming, Biostatistics, DIS, ITG, Medical Writing, RA and QA to ensure that data collected during trials are managed according to corporate standards and meet regulatory guidelines for data integrity.

Additional Responsibilities:

• Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.
• As a Manager, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Manage the Data Management team, study and or program of studies to ensure project objectives are met within budget, to agreed timeline and to high level of quality.
• Manage clinical data management staff as appropriate, including but not limited to resource planning, recruitment, performance evaluations and training.
• Develop and foster sponsor relationships through effective project management and communication.
• Provide regular status reports and KPIs to senior management and represent Data Management at oversight meetings.
• Manage the forecast and revenue recognition process by continuous review of monthly files and incremental review of project analysis files to meet departmental objectives for profit and margins.
• Represent Data Management at internal/external audits and manage findings through resolution both operationally and within the Quality Management system.
• Provide Project Management to Biostatistics and Medical Writing when Clinical Operations is not a function provided by ICON.
• Lead the development, implementation and maintenance of guidelines and procedures to facilitate the efficient performance of data management activities.
• Actively participate in departmental and company initiatives.
• Actively participate in the development of departmental specific training courses and conduct introductory led training courses for data management staff.
• Provide input into CRF design, protocol review, edit check specifications, data entry conventions, monitoring guidelines, and any other study related documents, as required.
• Actively participate in Business Development presentations to sponsors as required.
• Assist Business Development colleagues with the preparation of Data Management bids as required.
• Provide other general duties as required to support the company.

Supervision Field

• Develop supporting staff skills, encourage growth and provide regular performance feedback in one to one meetings and interim/yearly appraisals
• Manage staff and set clear goals and objectives
• Address performance issues promptly and devise a development plan to address areas for development.
• Effectively manage work priorities of self and direct reports, delegating responsibilities where appropriate
• Monitors compliance to ensure studies are in line with internal quality initiatives and that they are inspection ready
• Monitor compliance to Trackwise responses, PV timesheet, IDOC, iLearn to ensure no backlogs built

Experience and Qualification

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Proven experience in clinical data management or other relevant experience.
• Experience of at least one of ICON preferred CDMS (Rave, Inform, Oracle Clincal, OCRDC)
• Highly computer literate, including strong Microsoft Office skills (Excel, Word, PowerPoint, Project)
• Excellent communication and interpersonal skills, both verbal and written skills
• Strong client relationship management skills, and the aptitude to develop this further
• Excellent organizational and planning skills as well as a demonstrated aptitude for project management, and the ability to lead more than one project and prioritize accordingly

WHAT IS ON OFFER?

Come to ICON and be an important part of a well-respected and growing company that believes the details of your career are every bit as critical as the work you do. You will be valued for your passion, commitment, individual perspective and personal contribution to the success of this company. Successful candidates can enjoy all the benefits associated with working for a truly global company including a highly competitive benefits package. We also encourage work/life balance, offer training and development; provide flexible working arrangements, etc.

TO APPLY:

To apply for these roles - you must have appropriate rights to work and live in China. If you are interested in these exciting new opportunities, please send your resume (in Word Format ONLY) to:

Jerry Wang

Senior Recruitment Consultant - Greater China

Email: jerry.wang@iconplc.com

Phone: +86 10 8529 5100

ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.

A global leading company focus on the drug research, clinical research and providing Clinincal operation solution for world famous pharamcy company. We have over 9000 people all of the World and entered into China in 2005. Will with a good development plan to broaden and improve China business scale.