Jobs at Pharmavise Corporation

Conduct high-volume outbound outreach through email, LinkedIn, and phone to engage business development prospects, schedule discovery calls, and support lead qualification. Maintain accurate lead and activity records in Zoho CRM, coordinate pre-sales activities, prepare client briefing documents, and ensure qualified opportunities are handed off to business development managers. The role also supports talent pipelines and requires strong communication, organization, follow-up, and multitasking skills.

Manages clinical laboratory study maintenance, data lock, closeout, document workflows, budgets, sample and device tracking, query management, and data delivery. Serves as the primary CLS contact for study teams and third-party organizations while coordinating internal and external partners. The role requires advanced medical science education, extensive project or program management experience, and prior pharmaceutical, diagnostics, CRO, or clinical research experience.

Manages clinical laboratory study maintenance, data lock, closeout, document approvals, budgets, sample and device tracking, query management, and data delivery. Serves as the primary CLS contact for study teams and third-party organizations, collaborating with internal and external partners to support clinical research operations. The role requires strong organization, communication, attention to detail, clinical industry experience, and Excel proficiency.

Provides remote executive and administrative support, including calendar and inbox management, meeting coordination, proposal preparation, process documentation, CRM and database administration, SharePoint file organization, project coordination, vendor communication, and optional QuickBooks invoicing support.

Lead enterprise Quality Culture program across four cross-functional workstreams: assessment, action planning, stakeholder engagement, and education. Standardize assessments, analyze results, develop remediation plans, track implementation with dashboards, and drive global adoption through communication, training, and governance to improve quality behaviors and Cost of Quality.

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

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 role involves ensuring compliance with GMP regulations, conducting audits, providing GMP training, and collaborating with various teams to improve manufacturing processes.

Lead GxP-focused consulting projects, develop and optimize Quality Management Systems, support compliance readiness, mentor junior members, and provide expert regulatory advice.

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

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.

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

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.

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.

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

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

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

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

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

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.