Ora, Inc.

HQ
Andover, Massachusetts, USA
552 Total Employees
Year Founded: 1977

Jobs at Similar Companies

Similar Companies Hiring

Software • Pharmaceutical • Healthtech
12 Offices
69000 Employees
Telehealth • Social Impact • Pharmaceutical • Healthtech
New York City, NY
13 Employees
Pharmaceutical • Logistics • Healthtech
12 Offices
46000 Employees
Jobs at Ora, Inc.
Let Your Resume Do The Work
Upload your resume to be matched with jobs you’re a great fit for.

Recently posted jobs

Pharmaceutical
The Director of Business Development will lead the growth of target accounts and drive sustainable pipeline, managing complex negotiations and optimizing client relationships. Responsibilities include prospecting new business opportunities, networking, maintaining CRM systems, and representing the company at industry events.
2 Days Ago
Andover, MA, USA
Pharmaceutical
The Ophthalmologist at Andover Eye Associates will diagnose and treat various eye conditions, perform eye exams and surgeries, collaborate with other healthcare professionals, and engage in clinical research. They will provide comprehensive eye care, maintain medical records, and ensure data integrity in research studies.
7 Days Ago
Remote
United States
Pharmaceutical
As Corporate Counsel, you will provide legal support primarily to Business Development and Clinical Operations teams, reviewing and negotiating various commercial agreements. Key responsibilities include risk analysis, process improvement, contract template creation, mentoring non-attorneys, and ensuring compliance with legal standards and data integrity.
12 Days Ago
Remote
28 Locations
Pharmaceutical
The Director of Business Development (Europe) will enhance the growth of target accounts and drive a sustainable pipeline. Responsibilities include prospecting for new business, maintaining relationships with clients, monitoring leads, attending industry meetings, and ensuring compliance with regulations while adhering to Ora's values.
12 Days Ago
Hyderabad, Telangana, IND
Pharmaceutical
The Safety Specialist will prepare Safety Management Plans, Medical Monitoring Plans, and Safety reports for clinical trials. Responsibilities include quality checks on safety data, tracking Serious Adverse Events, and maintaining safety documentation in study files. The role involves collaboration with various teams for data management and ensuring compliance with safety protocols.