【外資系医療機器メーカー】Sr Mgr, Clinical Program Management

求人詳細

Lead and grow a high-performing clinical team in a dynamic and innovative medical device company.

■About the company
Our client is a global leader in the medical device industry, committed to developing cutting-edge technologies and improving patient outcomes. They foster a collaborative and supportive work environment where innovation and teamwork are highly valued.

■Role & Responsibilities
As a Sr. Manager, Clinical Program Management, you will be responsible for overseeing the successful execution of multiple clinical trials. You will lead and mentor a team, develop project plans, manage resources, and ensure compliance with GCP and regulatory guidelines. You'll also be a key stakeholder in strategic decision-making, influencing the direction of clinical development initiatives and presenting findings to executive leadership.

■Main tasks include
・Lead and mentor a team of clinical trial managers.
・Develop and manage comprehensive clinical project plans, ensuring timely completion of milestones.
・Oversee the selection and management of clinical vendors and study sites.
・Analyze trial performance and implement corrective actions to mitigate risks.
・Manage project budgets and resources effectively.
・Communicate effectively with internal and external stakeholders.
・Present trial information at executive and industry conferences.

If you are interested in this exciting opportunity, apply now.
We look forward to hearing from you.
#LI-Hybrid

こんな方を求めています

経験・スキル

■Requirements
・Bachelor's degree in a related field (e.g., life sciences, clinical research); Master's degree preferred.
・Minimum of 8 years of experience in clinical research, with at least 5 years in a management role.
・Proven track record of successfully managing and completing complex clinical trials.
・Expert knowledge of GCP, ICH guidelines, and relevant regulations.
・Experience with clinical trial management systems (CTMS) and eTMF.
・Strong leadership, communication, and interpersonal skills.
・Excellent analytical, problem-solving, and organizational skills.
・Proven ability to manage budgets and resources effectively.
・Experience with regulatory submissions and audits is highly desirable.
・Fluency in English is required; Japanese language skills are a plus.

学歴

大学卒業以上

募集要項

職種

臨床開発、CRA、CRC

給与

年収 1,000 〜 1,380万円

賞与

+16％

雇用形態

正社員

雇用期間

期間の定めなし

就業時間

09:00～18:00

休日休暇

土曜日　日曜日　祝日

保険

健康保険　厚生年金保険　雇用保険

受動喫煙防止措置

敷地内禁煙

業種

医療機器・医療品関連

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