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Remote Pharmaceutical Biomedical Engineer Jobs in Ohio

Bachelor's in informatics, computer science/engineering, biomedical engineering, health information ... pharmaceutical, and medical device industries. Our mission is to accelerate the global development ...

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right ... Solid SAS programming skills, including QC of critical outputs, efficacy and safety tables, and ...

Senior IP Counsel - Materials Group

Mentor, OH · On-site +1

$124K - $169K/yr

... pharmaceuticals and automotive -- we employ approximately 35,000 employees in more than 50 ... Mentor, OH (Hybrid preferred; remote work will be considered for qualified non-local candidates ...

Senior IP Counsel - Materials Group

Mentor, OH · On-site +1

$124K - $169K/yr

... pharmaceuticals and automotive - we employ approximately 35,000 employees in more than 50 countries ... Mentor, OH (Hybrid preferred; remote work will be considered for qualified non-local candidates ...

Showing results 21-36

Remote Pharmaceutical Biomedical Engineer information

What is a remote pharmaceutical biomedical engineer?

A Remote Pharmaceutical Biomedical Engineer is a professional who applies engineering principles to the design, development, and maintenance of medical devices, equipment, and processes used in the pharmaceutical industry, while working from a remote location. Their tasks may include developing new drug delivery systems, ensuring compliance with regulatory standards, and collaborating with cross-functional teams virtually. They use specialized software and communication tools to manage projects, analyze data, and contribute to the advancement of pharmaceutical products, all without being physically present at the company’s facilities.

What are the key skills and qualifications needed to thrive as a remote pharmaceutical biomedical engineer?

To thrive as a Remote Pharmaceutical Biomedical Engineer, you need a strong background in biomedical engineering, pharmaceutical sciences, and regulatory compliance, typically supported by a relevant degree. Familiarity with tools such as CAD software, laboratory information management systems (LIMS), and knowledge of FDA or EMA regulations is essential. Exceptional problem-solving, self-motivation, and effective virtual communication are crucial soft skills for remote collaboration and project management. These skills ensure the development of safe, effective biomedical products and seamless teamwork within geographically distributed pharmaceutical teams.

How does a remote pharmaceutical biomedical engineer typically collaborate with on-site teams and cross-functional departments?

As a Remote Pharmaceutical Biomedical Engineer, you will regularly collaborate with on-site teams, such as quality assurance, manufacturing, and research scientists, through virtual meetings, project management software, and shared documentation platforms. Effective communication and organization are essential to align project goals, address technical challenges, and ensure compliance with industry standards. You may also participate in cross-functional reviews, contribute to process optimization, and provide technical input for product development, all while coordinating closely with colleagues across different locations and time zones.

What are the most commonly searched types of Pharmaceutical Biomedical Engineer jobs in Ohio?

The most popular types of Pharmaceutical Biomedical Engineer jobs in Ohio are:

What cities in Ohio are hiring for Remote Pharmaceutical Biomedical Engineer jobs?

Cities in Ohio with the most Remote Pharmaceutical Biomedical Engineer job openings:

Clinical Informatics Analyst

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 21 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 rated research


Job description

Job Summary

Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering teams.

Responsibilities
  • Evaluate data needs for assigned projects and make recommendations on strategic approach specific to the study design;
  • Work alongside operational and medical leads to contribute innovative data products;
  • Interact with relational data at both study- and enterprise-level inclusive of actions for query, wrangling, analysis, and reporting;
  • Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and
  • Support departmental process improvement initiatives.
Qualifications

Qualifications

  • Bachelor's in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field;
  • Analytical thinker with great attention to detail;
  • Ability to prioritize multiple projects on a sprint schedule;
  • Excellent verbal communication skills;
  • Programming experience in R or Python;
  • Work experience with clinical data;
  • Experience building web applications is preferred (with either Shiny or Streamlit); and
  • Experience building dashboards is preferred (with either PowerBI, Tableau, or Spotfire).

Additional Considerations

We are hiring all levels of experience. Degree level, work experience, interview performance, and programming proficiency will be considered. Prior to the interview stage, a programming assessment will be conducted, details will be shared with candidates during scheduling confirmation.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

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Medpace logo

About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992