- Collaborate with the Medical and Safety Data Review teams to ensure timely progress and consistency with deliverables associated with medical data review (e.g., summary of clinical trial data) and, where appropriate, review of:
- Participate in the preparation of medical monitoring plans in collaboration with Drug Safety and Medical Data Review teams.
- Respond to protocol questions/CRAs/Sites under direction and supervision of the global study TMA.
- Collaborate with Project Leads and Contract Analysts to review and finalize the contract/budget and future COs.
- Prepare for and where required attend Safety review meetings with Sponsors under the supervision of the global Medical Advisor and the Medical Safety physician, covering areas such as:
- Coordinate activities and 'flow of information' with Medical Safety Advisor, Medical Data Reviewer and Medical Surveillance Specialist during study start up and throughout the project lifecycle, such as:
- Support quality assurance and other audits that involve the review of medical services (e.g., preparation of files, tracking and management of audit follow up actions and preventatives).
- Conduct electronic Trial Master File (eTMF) maintenance in relation to Medical and Scientific Services activities.
- Prepare and deliver presentation materials under the supervision and review of the global TMA, such as:
- Perform literature searches and summarize data/information including:
- Where appropriate, contributes to:
- Contribute to Medical and Scientific Services and other initiatives that support the advancement of IQVIA therapeutic capabilities
- Understanding of relevant therapeutic area
- Understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Knowledge and experience to conduct activities in compliance with regional/global regulatory requirements
- Understanding of clinical trial design and execution
- Good communication, interpersonal, negotiating and reporting skills
- Demonstrated proficiency in using systems and technologies to achieve work objectives
- Medical/clinical knowledge to independently review adverse event data
- Ability to work on and collaborate with colleagues on global teams
- Ability to proactively predict issues and solve problems
- Ability to positively influence internal and external stakeholders, including internal global and matrix teams
- Ability to balance multiple priorities
- Master's degree in a biomedical, life science or similar scientific field 3 years of clinical trial experience, including 2 years of directly relevant therapeutic area(s) experience
- Advanced scientific degree preferred (PhD, PharmD)
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Clinical Trial Manager
Encontrado em: Buscojobs BR C2 - há 2 dias
Iqvia Llc São Paulo, BrasilClinical Trial Manager - Sponsor Dedicated page is loaded Clinical Trial Manager - Sponsor Dedicated Apply locations São Paulo, Brazil time type Full time posted on Posted 2 Days Ago job requisition id R Clinical Trial Manager The Clinical Trial Manager provides leadership of the ...
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Clinical Trial Manager
Encontrado em: Buscojobs BR C2 - há 3 dias
Iqvia Llc São Paulo, BrasilClinical Trial Manager - Sponsor Dedicated page is loaded Clinical Trial Manager - Sponsor Dedicated Apply locations São Paulo, Brazil time type Full time posted on Posted Yesterday job requisition id R Clinical Trial Manager The Clinical Trial Manager provides leadership of the ...
Clinical Scientist - São Paulo, Brasil - IQVIA
Descrição
PURPOSE
The Clinical Scientist supports medical monitoring and scientific tasks on projects under the guidance of Therapeutic Medical Advisors (TMA) and in collaboration with the cross functional project team. These activities enable the use of high quality, scientific data to make timely decisions during clinical study planning, execution, analysis, and reporting. This includes CRA/investigative site support as well as advanced safety and data analytics.
RESPONSIBILITIES
o Patient profiles
o Safety listings
o Other data listings, including Efficacy listings
o Coding for Adverse Events (AEs)
o Concomitant medications
o Safety listings review and queries generation, where appropriate
o Protocol Deviations Log review
o Concomitant medications and coding
o Participate in the preparation of information and summary slides for client mtg
o Manage and track action items from Medical Delivery Services Kick-off mtg
o Investigator meetings
o Protocol training
o CRA training
o Program kick-off meetings
o Disease area research
o Standard of care
o Results from clinical trials in specific indications
o protocol concept development by providing input to the Medical Writer
o clinical study reports by providing input to the Medical Writer
o clinical sections of Regulatory documents by providing medical team input
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at