掲載期間:22/09/02~23/03/01 求人管理No.020067

外資系CRO

Manager, Safety & PV (Line Manager)

  • 受託会社
  • 年間休日120日以上
  • フレックス勤務
  • 女性が活躍
  • 年収1,000万円以上
  • 管理職・マネージャー
  • 英語を活かす

募集要項

外資系大手CROでのPVマネジメント業務

仕事内容

Line management responsibilities including transfers, hiring, utilization, terminations, training, professional development, performance appraisals, time sheet approval, and employee counseling. Advises staff on administrative policies and procedures, technical problems, and prioritization.
Assigns project work and reviews workload for all direct reports. Provides oversight and guidance on organizational goals and company objectives.
Monitors quality of work and efficiency of team members with contracted scope of work and Safety Management Plan. Discusses below-target project goals with senior safety management.
Manages projects where Safety and Pharmacovigilance are the primary services.
Reviews study budgets and expenses; ensures all study related contractual and budgeting issues are upheld and performed.
Works with Finance to ensure appropriate customer invoicing, where required.
Approves project time cards and invoicing.
Provides sponsors with scheduled project updates and reports.
Coordinate with other internal departments and Safety functional areas to ensure timely review and submission of reports and documents relating to safety reporting as well as resolution of issues.
Participates in the management of the Safety and Pharmacovigilance department with the following actions:
Assists in the development, review, and approval of departmental Standard Operating Procedures (SOPs)
Reviews, provides input, and ensures the execution of the Safety Management Plan/Safety Reporting Plan.
Evaluates processes for potential improvement in efficiency and effectiveness and recommends changes. Participates in process development and improvement of departmental functions.
Works with Business Development to actively solicit new business, as needed.
Represents Safety and Pharmacovigilance or ensure Safety representation at project team meetings and client meetings.
Reviews, advises, and approves Safety portions of project proposals to ensure wording adequately reflects the scope of work for Safety and Pharmacovigilance. Participates in bid defense meetings. Reviews clinical safety sections of study protocols and Case Report Forms (CRFs) to make sure information is consistent with the Serious Adverse Event form. Approves budget projections for the project.
Maintains understanding and ensures compliance of SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCPs, ICH guidelines, GVP modules, study plans and the drug development process.
Responsible for the identification, preparation, and delivery of any necessary training to Safety team members and other departments or groups. Mentor Safety team members
Managing resourcing's needs/issues and escalating to senior management as necessary.
Participates in audits/inspections and ensures inspection readiness. Participates in quality investigations and implementation of corrective and preventive actions.
Performs other work related duties as assigned.
Minimal travel may be required.

応募条件
【必須事項】
BA/BS in the biological sciences or related disciplines in the natural science/health care field or nursing degree or equivalent combination of education and experience
Progressive responsibility with demonstrated leadership skills and project management
Clinical Research Organization (CRO) experience with therapeutic specialties preferred
Working knowledge of financial budgets and various financial analysis tools preferred
Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), TeamShare (or other management/shared content/workspace), and internet
Excellent oral, written, and interpersonal communication skills with strong graphic presentation skills
Ability to establish effective relationships with clients as well as team members
Ability to be flexible, adapt to change, work independently, as well as part of a team in a matrix environment
Ability to make effective decisions and manage multiple priorities while delivering high quality work in a dynamic environment
【歓迎経験】
【免許・資格】
【勤務開始日】
応相談
学歴
大学卒以上
雇用形態
正社員
試用期間
3ヶ月

契約期間
勤務地
東京
転勤の有無
転勤なし
受動喫煙防止措置
屋内禁煙
勤務時間
フレックスタイム制度あり:コアタイム10:00~15:00
休憩時間
60分
時間外労働
勤務開始日
応相談
休日休暇
完全週休2日制(かつ土日祝日) 有給休暇10日~20日 休日日数120日
年収・給与
年収  950万円~1250万円 経験により応相談
諸手当
交通費支給(上限月10万円)、出張手当、時間外勤務手当
昇給
年1回
賞与
年俸制
採用人数
若干名
待遇・福利厚生
【待遇】
<教育制度・資格補助補足> ・社内e-learningシステムINC Collegeによる各種研修プログラム ・英教育最大手ピアソンが提供するGlobal Englishの無料受講
【福利厚生】
選考プロセス
1)書類選考
2)一次面接
3)最終面接

外資系CRO

Manager, Safety & PV (Line Manager)

  • 受託会社
  • 年間休日120日以上
  • フレックス勤務
  • 女性が活躍
  • 年収1,000万円以上
  • 管理職・マネージャー
  • 英語を活かす

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