|給与||500万円 ~ 1500万円|
I am currently seeking an experienced Global Clinical Project Manager to join an International CRO, specifically focused in Europe and APAC.
The ideal candidate will speak English and Japanese, and will have approx 2/3 years of experience in global clinical trials.
The Project Manager manages the project team in the delivery of quality clinical trial management services to achieve the successful overall project completion. The PM will be expected to maintain an in-depth understanding of customer needs within the project group, to focus on achieving the project’s goals and to have knowledge in the assigned therapeutic area. According to his/her knowledge and skills the PM may take over any other tasks, duties, roles and job responsibilities at the discretion of the company and relevant managers.
The PM will provide a customer focused leadership role and may be assigned to manage multiple Phase I through Phase IV clinical research trials across all functional areas. The role holder will assure the understanding and integration of all functions, roles and responsibilities within the clinical project team and will effectively coordinate and manage cross functional teams that deliver clinical projects (Clinical Monitoring, Data Management, Biostatistics, Medical writing, Pharmacovigilance, Regulatory) including vendors, if applicable.
The PM will monitor adherence to project contract and budget. In addition the PM is expected to assist with proposal generation within a multifunctional matrix setting. The PM is expected to assist in business development activities to achieve high level of customer satisfaction and therefore ensuring repeat business opportunities.
University/college degree in a life science field (Master’s or other advanced degree is preferred) or equivalent experience or equivalent education.
At least 5 years of clinical research experience in a CRO, biopharmaceutical company or relevant clinical environment and a minimum of 2 years in team leader function (e.g. Monitor Lead (ML)) or equivalent study coordination or management experience. Experience in study management in Japan and/or an Asian country (e.g. Taiwan, Korea) is required. Clinical operations management experience (e.g. ML) is required.
In depth knowledge of the clinical trial process and CRO industry is mandatory for this function.
Outstanding written and oral English and Japanese skills are required to qualify for this role. An additional language is a plus.
|給与||500万円 ~ 1500万円|
|会社の種類||大手企業 (300名を超える従業員数) - 外資系企業|