Clinical Affairs Jobs

Clinical Scientist Undergraduate

**Department Overview** (The Vaccine Medical Development, Scientific / Clinical Affairs Global Team has staff located in the US and Europe and assists with the clinical development of Vaccine’s across the globe. The Clinical Scientist provides medical, scientific and clinical study and project support for multiple, global, Phase 4 vaccine clinical and epidemiology studies in a […]

Clinical Research Associate

The Clinical Research Associate prepares and executes clinical operations study tasks, including: documents (may include plan, protocol, report); initiation, monitoring, and completion of clinical studies for verification and/or validation. This position represents the Global Clinical Affairs group on multi-functional core teams to ensure project requirements are met and clinical trials are conducted successfully. Ensures adherence […]

Electrical Engineer

null **In this role, you have the opportunity to:** Help create a healthier society through meaningful work. Philips is the leader in Image-Guided Therapy, providing integrated solutions that advance minimally invasive procedures. We help healthcare providers to decide, guide, treat and confirm the right care in real time during the procedure to enable better outcomes […]

Medical Manager

**Purpose:** The Medical Manager is instrumental in developing and implementing medical and other value-creating strategies from key insights obtained from stakeholder engagements and partnerships. Key functions will include customer engagement and insight generation, stakeholder management, data generation, medical operations and compliance oversight. The medical manager aligns with internal stakeholders such as other medical affairs colleagues, […]

Expert Regulatory Specialist

null **In this role, you have the opportunity to** + Provide expert regulatory support for Image Guided Therapy and execute PMAs for implantable devices in the US, EU MDR transition. + Be recognized as a Regulatory Expert in US, EU, and other regional Regulatory filings. + Be considered a vital regulatory point person in multiple […]

Post Market Surveillance Manager

null **In this role, you have the opportunity to** The Post-Market Surveillance team is responsible for monitoring, investigating, tracking and reporting on the performance of all Hospital & Respiratory Care products in the field. This activity is undertaken primarily through the management of the Complaint Handling System. The team is responsible for global vigilance reporting […]

Engineering Program Manager

Essential job responsibilities: + Leads the planning and implementation of multiple Hardware/Software/Instrument Engineering development programs, with full responsibility for the project from both business and technical perspectives. + Lead cross-functional core teams including team members from departments such as Biology, Engineering, Marketing, Regulatory, Clinical Affairs, Quality, Manufacturing, Supply Chain, and others in the planning, coordination, […]

Medical Advisor, Hospital BU

LOCATION: Mumbai, Hyderabad, Chennai, Bangalore MAIN REPONSIBILITIES / DUTIES + Medical Strategy Development /Policy shaping + To develop and lead the implementation of the medical strategy for the Hospital Business Unit (HBU) + Provide medical support towards business development, new product launches, and stewardship initiatives. Will be ultimately accountable for the medical and regulatory strategy […]

International Regulatory Affairs Specialist

null **In this role, you have the opportunity to** + Configure and deploy document management processes and tools related to global regulatory submissions + Compile Regulatory filings for EU MDR and roll them out in Worldwide. + Be recognized as a key talent in the implementation of the European Medical device Regulation 2017/745 in a […]

Label Specialist

null **In this role, you have the opportunity to** Bring your passion and energy into a growing department dedicated to the quality output of product labeling and packaging for Image Guided Therapy (IGT) devices in accordance with GMP’s, FDA Regulations, EUMDR, ISO Requirements and Standard Company Operating Procedures. **You are responsible for** + Develop and […]

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