Position is virtual and will be working on UK / US hours. 8PM to 5am PH Time
Qualifications:
- Bachelors degree with at least 5 years of experience; OR a masters degree with at least 3 years of experience; OR a PhD with 0 years of experience; OR as associates degree with 8 years of experience;
- Bachelors degree in supply chain scientific discipline project management or business administration
- 5 years of experience in pharmaceutical or biotech project management and cross-functional team leadership
- Demonstrated understanding of pharma quality and regulatory framework.
- Demonstrated success in matrix team environments with strong collaboration and accountability
- Excellent English communication skills (written and verbal)
- Proficiency in Microsoft Office tools including MS Project and Office Timeline-Pro
- Flexibility to work across global time zones
Skills:
- Knowledge of Good Manufacture Practice (GMP) Good Clinical Practice (GCP) and regulatory frameworks
- Proven ability to manage complex clinical development programs and multiple studies
- Background in drug development or clinical study logistics (e.g. randomization packaging labeling distribution)
- Strong budgeting and forecasting skills including supply demand planning
- Skilled in stakeholder alignment negotiation and performance measurement
- Experience presenting at conferences or large forums
Preferred:
- Business scientific or technical degree and/or coursework with specific training in supply chain management preferably in pharmaceutical industry.
- Training or experience in safety regulatory medical and/or clinical supply chain delivery and/or implementation.
- In-depth understanding of pharmaceutical business processes and regulations guidelines and industry standards for compliance.
- Proven ability to effectively develop communicate and execute project plans with multiple stakeholders.
- Previous continuous improvement experience considered a plus.
- Strong interpersonal skills with a demonstrated ability to manage stakeholders in different levels of technical and business roles.
#LI-CES
#LI-PK1
#LI-DNP
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.
Position is virtual and will be working on UK / US hours. 8PM to 5am PH TimeQualifications:Bachelors degree with at least 5 years of experience; OR a masters degree with at least 3 years of experience; OR a PhD with 0 years of experience; OR as associates degree with 8 years of experience;Bachelors ...
Position is virtual and will be working on UK / US hours. 8PM to 5am PH Time
Qualifications:
- Bachelors degree with at least 5 years of experience; OR a masters degree with at least 3 years of experience; OR a PhD with 0 years of experience; OR as associates degree with 8 years of experience;
- Bachelors degree in supply chain scientific discipline project management or business administration
- 5 years of experience in pharmaceutical or biotech project management and cross-functional team leadership
- Demonstrated understanding of pharma quality and regulatory framework.
- Demonstrated success in matrix team environments with strong collaboration and accountability
- Excellent English communication skills (written and verbal)
- Proficiency in Microsoft Office tools including MS Project and Office Timeline-Pro
- Flexibility to work across global time zones
Skills:
- Knowledge of Good Manufacture Practice (GMP) Good Clinical Practice (GCP) and regulatory frameworks
- Proven ability to manage complex clinical development programs and multiple studies
- Background in drug development or clinical study logistics (e.g. randomization packaging labeling distribution)
- Strong budgeting and forecasting skills including supply demand planning
- Skilled in stakeholder alignment negotiation and performance measurement
- Experience presenting at conferences or large forums
Preferred:
- Business scientific or technical degree and/or coursework with specific training in supply chain management preferably in pharmaceutical industry.
- Training or experience in safety regulatory medical and/or clinical supply chain delivery and/or implementation.
- In-depth understanding of pharmaceutical business processes and regulations guidelines and industry standards for compliance.
- Proven ability to effectively develop communicate and execute project plans with multiple stakeholders.
- Previous continuous improvement experience considered a plus.
- Strong interpersonal skills with a demonstrated ability to manage stakeholders in different levels of technical and business roles.
#LI-CES
#LI-PK1
#LI-DNP
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.
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