Summarized introduction:

PPD is proud to employ over 20,000 employees worldwide, across 47 countries and 89 offices. In just over 30 years, PPD has grown to become a leading U.S. based CRO and recently has won accolades for industry leading CRA team, employee training & development, excellence in service and numerous awards for Best CRO. Our sustained year on year growth means that we are always looking for exceptional clinical talent to join our company.

PPD China is looking for experienced Physicians to join our team. If you are a physician with more than 5 years’ experience inon internal medicine, especially Oncology, and good English presentation skills, please do not hesitate to contact us. We can offer you high-quality global studiesy, and a competitive salary package with homebased chance in China!

Job responsibilities:

Manages all medical aspects of contracted tasks across the pharmaceutical product

life-cycle.

General Support:

• Ensures tasks delegated to PVG Pharmacovigilance are properly executed.
• Provides medical consultation to team members and answer all study related medical questions.
• Provides therapeutic training and protocol training on assigned studies, as requested.
• Assists in writing (interpretation of safety and efficacy data) .

Clinical Trial Support:

• Monitors all safety variables of clinical studies.
• Discusses all medical concerns with principal investigators and clients raised during the course of a study, using proper medical judgment in the interpretation and decision making with regard to clinical situations as they relate to the investigational study.
• Provides medical review of adverse events of special interest, serious adverse events and clinical outcomes events reported by study sites.
• Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess for potential safety concerns.

Marketed Products Support:

• Manages signal detection activities, scientifically reviews aggregate reports, contributes to label updates, supports dossier maintenance and risk management activities.
• Medically reviews adverse event and serious adverse event data from all sources as contracted.

Qualifications:

Education and Experience:

MD MBBS or equivalent requirededucation. Active Medical license.medical licensure preferred. Candidates should have at least one of the following:

? Clinical experience in treating patients in Internal Medicine indications, ideally Oncology the speciality or sub-speciality associated with the applicants training (comparable to 2 5 years); Or

? Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or

? Direct experience in safety/Pharmacovigilance (comparable to 2 years).

Knowledge, Skills and Abilities:

• Therapeutic expertise across one or more medical specialityspecialty or sub-specialitiesspecialties
• Strong decision-making, problem solving, organizational skills and analytical skills
• Excellent oral and written communication skills
• Working knowledge of relevant safety databases (e.g. Medra)
• Flexibility to travel domestically and internationally
• Ability to work independently, analyze work with attention to detail, process and prioritize sensitive complex information

Our offer: As a compensation, you will be provided with a competitive remuneration, corporate trainings and the opportunity to become a part of a fast growing, multinational company. At PPD, we encourage our employees to demonstrate creativity, innovation and fresh insights as well as a solution-focused approach. We also value teamwork, camaraderie and enthusiasm. This is a full-time, permanent position.

Locations we are hiring in are:

• Office based Beijing
• Office based Shanghai
• Homebased in other Chinese cities

上班地址：东直门南大街1号来福士大厦