成長著しい外資製薬会社の開発本部においてAssociate Clinical Operations Managerを募集いたします!成長著しい外資製薬会社の開発本部においてAssociate Clinical Operations Managerを募集いたします!

求人情報


成長著しい外資製薬会社の開発本部においてAssociate Clinical Operations Managerを募集いたします!

求人番号 26103
会社名 外資製薬会社
業種 製薬
職種分類 臨床開発(CRA/統計・DM/QC・QA/臨床企画)
ポジション Associate Clinical Operations Manager
仕事内容 【主な役割】
Monitors activities conducted by clinical investigative sites as they relate to clinical studies to ensure successful execution of the protocol. This position function in an off-site and affiliate based capacity.
The Associate Clinical Operations Manager(ACOM) conducts clinical site monitoring visits across a maximum of 5 protocols and multiple therapeutic areas, ensuring studies are conducted accoring to all applicable regulations and business processes. Ensure regulatory inspection readiness at assigned clinical sites. May be responsible for assignments of greater complexity than the Clinical Research Associate(i.e., greater number of sites, site participating in more complex clinical studies, sites requiring more oversight of operational issues).
Additionally, the ACOM may trrain and provide guidance to junior staff.

Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
Supports the Clinical Operations Manager (COM) and/or Senior Clinical Operations Manager (SrCOM) in the
provision of leadership and oversight for activities undertaken by Clinical Operations (CO) Site Management &
Monitoring personnel in charge of implementing and monitoring clinical studies conducted within country (ex-US)
/ region (US) of responsibility.
In the country/region based, may manage up to 6 SCRAs responsible for site identification, qualification,
initiation, interim monitoring and study close-out visits for Phase 1-4 studies.
Gives support in providing ongoing assessment of resource needs and in allocating resources in alignment with
AbbVie’s research goals, priorities and specific study timelines. Identifies and communicates issues that impact
resource allocation and provides solutions.
For direct reports, ensures clinical monitoring activities are conducted according to the monitoring plan and are in
accordance with project timelines and company objectives. Anticipates and identifies site issues that could affect
timelines and develops alternative solutions.
Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in
accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard
Operating Procedures (SOPs) and business processes.
Conducts all clinical site monitoring activities according to the monitoring plan and in accordance with the study
timelines and company objectives. This includes but is not limited to:
Manages and monitors the activities of clinical investigative sites across a maximum of 5 protocols and multiple
therapeutic areas with the ability to manage, with minimal supervision, sites participating in more complex
clinical studies and/or sites requiring more oversight of operational issues, than those assigned to (Sr) SCRAs.
Overviews the overall activities of site personnel over whom there is no direct authority and motivate/influence
them to meet study objectives.
Is proactive in managing the site and ensures action plans are put in place as needed to ensure compliance.
Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate
reporting and follow-up for all safety events by site personnel.
Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie
SOPs, ICH Guidelines, and applicable regulations.
Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent
project team members.
Appropriately reports and escalates serious or outstanding issues to project team member(s) and/or Senior
ACOM/ COM/ Sr COM as appropriate, as defined in the study monitoring plan.
Facilitates Quality Assurance Audit processes as indicated.
Ensures regulatory inspection readiness at assigned clinical sites.
Implements appropriate activities to ensure the site meets the enrolment target within the agreed timeline by
enhancing the enrollment schedule of clinical investigative sites.
Reviews monitoring visit reports for assigned CRA’s. May act as back-up or secondary reviewer for other countries
as required.
Reports monitoring activities and study site conduct accurately and completely. Prepare and submit written
reports, both monitoring and administrative, in a timely, concise and objective manner.
Participates in field training and mentoring of new/junior SCRAs as well as insourced SCRAs. May provide input
relative to performance review and development opportunities.
Proactively identifies issues that may impact enrollment and recruitment timelines, and provide objective
comments regarding these issues.
Collaborate with senior staff to develop initiatives and contingencies to ensure that timelines are met.
Prepares CA (Country Agency) and/or EC (Ethical Committee = IRB) documentation, ensures submissions and/or
notifications are performed as applicable. Manage and liaise with appropriate functions to respond to CA and/or
EC questions and related follow-up.
May coordinate local SCRA team working on the same projects, when applicable.
Supports remote monitoring, if and as applicable.
Employs excellent financial management to conserve costs of departmental operation and controls travel
expenses, with guidance from Senior ACOM/ COM/ Sr COM as appropriate.
Provides hands-on assistance to assigned staff for project implementation as needed. Where appropriate, monitors
project progress against time frame and budget. Informs the Clinical Operations Manager and/or the Senior
Clinical Operations Manager of any variance.
Supports the Clinical Operations Manager and/or Senior Clinical Operations Manager in ensuring that globally
accepted compliance standards are met in the country based, and that quality standards in the conduct of clinical
research are maintained.
Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH
Guidelines, and AbbVie Standard Operating Procedures (SOPs) and to quality standards in conducting clinical
research.
Manages investigator payments as per executed contract obligations.
Negotiates investigator/ hospital agreements with stakeholders
Maintain and complete own expense reports as per local and applicable guidelines.
Identifies, evaluates and recommends new/potential investigators/sites on an on-going basis. Potential sites may
be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies
with qualified investigators.
Participates in and/or presents at departmental and other functional meetings as needed, including Site
Management & Monitoring meetings.
Participates in special projects/work groups.
Identifies and partners with other AbbVie personnel to develop innovative processes and technologies to increase
the quality, productivity, and efficiency of Clinical Operations while conserving overall departmental operating
costs.
Maintains knowledge and expertise across multi-therapeutic areas through clinical and scientific literature
review, ongoing awareness and trends of industry practices and participation in professional activities.
Creates a positive work environment by encouraging mutual respect, innovation, and accountability at all levels.
Maintains appropriate communication with relevant functional areas.
Undergoes and maintains training as required by Global Clinical Operations and other relevant company
procedures, to ensure adherence to federal regulations, Good Clinical Practices (GCPs), ICH Guidelines, and
AbbVie Standard Operating Procedures (SOPs) and business processes.
Typically based in a large business unit to support the Clinical Operations Manager.
Typically responsible for a number (1–6) of monitoring staff within one country/region while keeping some site
management (CRA-) responsibilities.
Uses multiple technologies to maintain open and frequent communication with internal & external customers.
Interacts with, builds and maintains professional and collaborative relationships with:
- Study personnel (investigators, study coordinators, pharmacists, etc)
- Peers within the organization
- Study Teams/ Document Management
May interface with:
- Local personnel including Medical Department personnel and other AbbVie personnel within Clinical
Operations as well as Safety Representatives, Regulatory, Finance and Legal Functions, Human Resources,
administrative staff and other relevant functional areas.
External service providers
応募条件 ・薬学、生物学、化学、薬理学、その他関連する学問領域の学士か、同等以上の能力を有する。(修士、博士の学位があれば尚可)
・MS, MA, MBA, MPH desired
・Minimum of 5 years clinical related experience, with a minimum of 2 years as clinical research monitor.
・Experince in on-site monitoring of investigational drug in multi-therapeutic areas desired.
求める人物像 ・Excellent communication and interpersonal skills, including situations of conflict resolution, problem solving and crisis management. Demonstrated proactive and positive team player.
・Exhibits high level of flexibility when facing changes in the work environment.
・Acute observational skills, analytical and conceptual capabilities.
・Strong ability to work independently in a geographic region with minimal supervision.
必要スキル ・Expert knowledge and understanding or appropriate therapeutic indications as they relate to the conduct of clinical trials.
・Expert knowledge of regulations governing clinical research, ICH/GCP Guidlines and applicable regulations.
・Proven strong site management and monitoring skills.
・Exhibits strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.
・Current in-depth knowledge and understanding of appropriate therapeutic indigations as they relate to the conduct of clinical trials.
・Good negotiating skills, tact and diplomacy.
・Storong ability to work independently in a geographic region with minimal superbision.
・Working knowledge and high experience with electoric data capture systems and clinical trials management systems.


【英語スキル】
・ビジネスレベルの英語力

【ITスキル】
・Proficiency in the use of personal computers, including experiences with word processing, spread sheets, email and web-browser applications.

年収 900万 ~ 1250万
雇用形態 正社員
勤務地 東京本社
勤務時間 8:45~17:30
福利厚生 【待遇】各種社会保険等完備、退職金、団体生命保険、定期健康診断、自己啓発支援制度、社員持株会、財形貯蓄、医療費補助制度、永年勤続表彰制度、福利厚生プログラム、自動車通勤不可、TOEIC受験料補助
休日休暇 完全週休2日制、年間休日125日
募集背景 組織強化のため。
担当者 山本 俊輔
担当メッセージ 成長著しい外資製薬会社の開発本部においてAssociate Clinical Operations Managerを募集いたします!
臨床開発経験が豊富な方を求めています。
他の求人を検索 この求人に応募する(無料)
前のページに戻る

新着求人情報

キャリアコラム