Jobs at Pharmavise Corporation

The Clinical Research Manager oversees clinical trials management, ensuring compliance with regulations while leading cross-functional teams and managing budgets and timelines.

The Executive Assistant role involves managing executive calendars, communications, proposals, and documentation while supporting operational initiatives in a consulting firm.

The role involves providing regulatory guidance, assisting in FDA submissions, conducting assessments, and collaborating with clients and teams to ensure compliance with FDA regulations.

The Talent Acquisition & Business Development Representative role involves outbound outreach, appointment setting, and pipeline support for business development and recruitment in the life sciences consulting sector.

The Clinical Project Manager leads clinical trials, ensuring compliance with regulations, managing project plans, timelines, and budgets, while coordinating with teams and vendors.

The Clinical Data Manager oversees the quality and integrity of clinical trial data, ensuring compliance with protocols and regulations while collaborating with various teams.

Seeking an Electrical Engineer for design/testing of medical device components. Role involves DVT, data analysis, and collaboration with multiple teams.

The R&D Engineer will design and optimize medical devices, ensure regulatory compliance, conduct testing, and collaborate across teams to meet project requirements.

Lead medical device projects ensuring compliance with regulations. Collaborate with cross-functional teams for planning, execution, risk management, and reporting.

The Clinical Research Associate will manage study maintenance and closeout activities, liaise with study teams and external partners, and monitor clinical data and safety metrics.

The EU Generalist manages EU regulatory compliance, advises on product development and submissions, collaborates across teams, and stays updated on regulatory trends.

The Biostatistician designs, analyzes, and interprets clinical trial data, collaborating with various teams and ensuring statistical rigor and compliance with regulatory standards.

The Quality Engineer ensures products comply with medical device regulations, supports design control, conducts risk management, and participates in validation processes, audits, and improvement initiatives.

Provide expert consultation on bioequivalence studies, review protocols, oversee study designs, conduct analyses, and collaborate with teams to ensure compliance and execution of bioequivalence programs.

The Project Manager will lead cross-functional projects in life sciences, develop project plans, manage budgets, and ensure compliance with GxP and FDA regulations.

The UX/UI Designer will create compliant digital experiences for medical devices, leading design processes, collaborating with teams, and conducting user research to validate designs.

Lead GxP consulting engagements, optimize Quality Management Systems, provide compliance guidance, and mentor junior staff in the life sciences industry.

Serve as the primary clinical expert, provide guidance in clinical development, monitor trials, analyze data, and collaborate with teams to ensure compliance and patient safety.

The Contract Administrator will support contract development, review, and negotiation activities in the medical device industry, managing clinical study agreements and vendor contracts while collaborating with various teams to ensure compliance and efficiency.