Associate Director
Há 3 dias
Job Summary:
We are seeking a highly skilled Associate Director to lead our medical review team. The successful candidate will have extensive experience in pharmacovigilance and risk management, as well as strong leadership and communication skills.
Responsibilities:
- Lead the medical review of serious adverse events and nonserious adverse events from clinical trials and postmarketing surveillance
- Collaborate with project physicians to identify drug safety issues and prepare Aggregate Reports required by global regulatory agencies
- Participate in signal detection and evaluation activities and prepare Ad Hoc Reports reviewing specific safety issues
- Provide mentoring and indirect supervision of Senior Drug Safety Associates and Drug Safety Associates
Requirements:
To be considered for this role, you must have:
- A MD or DO degree with at least one year of postgraduate training or equivalent
- At least 2 years of experience working in related fields such as QA, Regulatory Affairs, medical writing, PCS, TM or clinical medical monitoring
- Strong communication and interpersonal skills
- Ability to work independently and in teams
Benefits:
- Opportunity to work on challenging projects with a global impact
- Competitive compensation and benefits package
- Professional development opportunities
About Us:
We are an equal opportunity employer committed to diversity and inclusion. We welcome applications from qualified candidates who share our values.
-
Assoc Medical Dir
Há 4 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroResponsible for medical review of serious adverse events and nonserious adverse events from clinical trials and postmarketing surveillance in support of drug safety activities for clients. - Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed to identify drug safety issues in collaboration with the...
-
Assoc Medical Dir
Há 3 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroResponsible for medical review of serious adverse events and nonserious adverse events from clinical trials and postmarketing surveillance in support of drug safety activities for clients.- Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed to identify drug safety issues in collaboration with the...
-
Associate Project Manager, Start-up
Há 5 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroGENERAL - Lead start-up team during study start-up phase liaising directly with Lead SUPM or Project Lead, core team members and the client, as applicable. - Serve as client’s contact for start-up and maintenance processes and oversight. Responsible for establishing a strong working relationship with client’s project teams. - Monitor and control start up...
-
Associate Project Manager, Start-up
Há 3 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroGENERAL- Lead start-up team during study start-up phase liaising directly with Lead SUPM or Project Lead, core team members and the client, as applicable.- Serve as client's contact for start-up and maintenance processes and oversight. Responsible for establishing a strong working relationship with client's project teams.- Monitor and control start up...
