Abbott
Associate Clinical Project Manager
United States - California - Sylmar
Sponsorship not specified$90k-$180kDetected 4 hours ago
GCPStatisticsProject ManagementHRISClinical TrialsClinical ResearchFDA RegulatoryMedical DevicesResearchCommunicationPublic SpeakingRegulatory Affairs
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Lottery odds (Level III)83
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About the role
- Provides project management expertise throughout the development and implementation of clinical studies.
- Is also assigned to other non-trial related activities such as process and procedure teams.
- Facilitates site selection process by conducting meetings with appropriate departments and individuals to review and revise draft site list as necessary, and by communicating the final site list to team members.
Responsibilities
- Interacts with various study support groups and the business unit in order to assist in clinical strategy, the development of study plans, and project deliverables.
- May support and mentor junior-level project managers.
- Facilitates the development of clinical strategy and trial design by conducting meetings with the appropriate departments and individuals to obtain feedback/direction.
- Provides input to protocol design, case report form design, data management plan, monitoring plan.
Nice to have
- Exercises authority and judgment to determine appropriate action.
- Demonstrates diplomacy and respect for others.
- Acts as a buffer for the team, providing focus and appropriate prioritization.
- Facilitates decision making.
- Demonstrates ability to influence others to achieve positive results and collaboration.
- Excellent knowledge of ISO and local regulations and required for clinical trials.
- Proven record of compliance with, and enforcement of, regulations in clinical trials.
- The base pay for this position is
Skills
- Abbott is a global healthcare leader that helps people live more fully at all stages of life.
- Our 115,000 colleagues serve people in more than 160 countries.
- Works with Study Team to coordinate activities for all milestones; database locks, annual reports, presentation and publications
Compensation
- Works with Study Team to coordinate activities for all milestones; database locks, annual reports, presentation and publications
Benefits
- Bachelors Degree (± 16 years), Preferably in Life Sciences OR an equivalent combination of education and work experience
- Minimum 5 years, Medical devices, clinical research experience, or related industry.
- Prefer at least 3 years of related work experience in Quality role in medical device area and/or clinical trial environment.
Equal opportunity
- Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
- EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
- EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
This listing is sourced directly from Abbott's careers page and normalized into a canonical job model.