Max Rate is (USD)123/hour
Would like someone on-site for this role
BIG TICKET ITEMS for this role:
Strong written and verbal communication and working with global teams – setting clear expectations, ensuring proper follow-up etc
Effective vendor management skills
PMP certification
Must have high level global experience.
The CTOM is responsible for the overall operational planning and activities for the implementation and conduct of studies (clinical trials, observational studies, compassionate use and registries) including oversight of data management activities in compliance with GCPs, SOPs and standards within established timelines and budgets.
The CTOM is involved in the scientific conduct of the study and acts as the leader of operational disciplines to guarantee release of homogeneous high quality data, in close collaboration with other functions (e.g. Medical Operations, Monitoring Team, Biostatistics) and with the CRO, for outsourced trials.
Capable of interacting effectively with scientists, support functions, subject matter experts and managers within and outside department; serve as internal consultant on assigned area and liaise with external organizations on projects.
- Strong interpersonal and communication/ presentation skills (verbal and written);
- Ability to handle multiple tasks and to prioritize, strong organizational skills
- Leadership & Project Management skills; positive, “can do” attitude, includes effective vendor and stakeholder management, risk management planning, active and effectual oversight of CROs,....
- Decision-making and problem-solving skills
- Ability to work autonomously and to efficiently & effectively provide status reports
- Ability to anticipate, identify and timely escalate issues and to define appropriate action plans
-Ability to anticipate, identify and mitigate risks, including their likelihood, scope and impact and to develop CAPAs
- Good cross-functional team leader who fosters team spirit and team motivation (team work)
- Knowledge and qualification with international standards (e.g. GCP, CDISC, etc.), company tools (including data management systems), processes and SOPs
- Experience in managing and leading international meetings (Clinical Trial Team, expert meeting, etc)
- Ability to work in an international environment with internal and/or external partners (CROs etc)
- Strong English skills (verbal and written if English is the second language)
- Ability to adapt and be flexible to change and managing internal and external impediments
- Understanding of database concepts preferred
Skills:Skills
10 years of experience in pharmaceutical industry or clinical-related discipline including at least 7 years clinical research experience, including 4 years of strong trial operations management experience across all study periods (start-up, maintenance and closure).
Strong written and verbal communication and working with global teams – setting clear expectations, ensuring proper follow-up etc
Adept in eDC systems – RAVE
Data Managemement experience
Effective vendor management skills
Education:.
Bachelor's degree Required
Languages:English Read Write Speak
Attachments: •
Last updated on Jul 7, 2016