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| Entreprise: |
ICON |
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| Intitulé: |
Associate Director/Clinical Operations |
| Secteur de l'Emploi: |
l'industrie Pharmaceutique |
| Localisation de l'emploi: |
Warszawa - Pologne |
| Ref.Emploi Numéros à conserver: |
AssDPO |
| Description: |
Do you empower those around you?
Can you offer a wealth of international Project Management experience?
ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support clinical development.
We are now looking to recruit a talented and dynamic Associate Director of Clinical Operations. We want to hear from you if you can demonstrate Clinical Project Management/Project Director experience through phases II-IV and are based in Poland.
1. Purpose Of The Job:
• To coordinate and manage the activities of individual studies and staff in a manner that ensures all timeframes and targets are met and that costs are kept under control.
• To effectively manage assigned staff to ensure high performance, continuous development and low turnover.
2. JOB FUNCTIONS
• Manage projects in a timely manner in adherence with ICON SOPs, ICH GCP and appropriate regulations and liaise with other department managers as necessary to achieve this.
• Develop and maintain a detailed Project Plan.
• Manage projects in accordance with the contract. Proactively recognise any changes in scope and collaborate with Business Development (BD) to ensure timely completion of change orders.
• Effectively manage the study budget to ensure financial targets are met through regular review of indirect costs and project resources. Collaborate with Finance to ensure accurate revenue recognition.
• Implement QC procedures and monitor quality metrics to ensure a high quality standard is maintained throughout the project.
• Act as the key client contact for designated projects and develop successful working relationships with clients.
• Ensure all necessary training is provided to his/her staff to improve their job performance and knowledge. Provide coaching/mentoring, as necessary.
• Effectively manage staff through open and timely sharing of information, regular performance review and feedback, and setting clear goals and objectives.
• Ensure time management system is up to date and monitor workload for assigned Clinical Research Associates (CRAs). Proactively flag potential resource issues to Director of Clinical Operations
• Provide regular feedback to senior management on project status, client satisfaction and staff issues.
• Participate in interviews, as required.
• Mentor Associate Clinical Project Managers/Clinical Project Manager Grade I’s, as appropriate
• Liaise with other managers to improve the effectiveness of the organisation.
• Maintain confidentiality of management information, as appropriate. Participate in BD activities, as appropriate.
• Participate in the Out of Hours on-call pager rota, as required.
3. Qualifications/experience Required:
• Background in medicine, science or other relevant discipline and proven project management track record.
• Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials.
• Good understanding of project management processes.
• Strong people management and effective communication skills.
• Good commercial awareness and customer focus.
• Fluent in written and spoken English and Polish.
• Computer literate.
• Current full driving licence.
• Ability and willingness to travel at least 35% of the time (international and domestic).
ICON can offer you:
• A company that accommodates innovative thinking – share ideas that will make a difference to the way we work
• Encourages staff to speak their minds – we want to know what you think
• Listens to views and suggestions that can make a difference – we welcome suggestions and views
• Work as one team with a common goal
• A commitment to quality – we are driven by quality
• Professional, friendly culture – that is fast paced and relaxed
• Challenging and rewarding
• Work hard but have fun too
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| Capacités Requises: |
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| Langues Requises: |
Anglais-Très BonAutres: Polish
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| Type de Contrat: |
Temps Plein
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| Salaire Annuel: |
Non spécifié
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| Date d'Affichage: |
jun 17 2008 |
| Niveau de Formation requis: |
Licence
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| Expérience (en années): |
5 à 7 Ans |
| Entreprise: |
ICON |
| Nom: |
ICON |
| Méthode de Contact Préférée: |
E-mail via l'encadré Postuler En Ligne |
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