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Biotech Application Jobs in Maine (NOW HIRING)

BioMed Engineer I

Lewiston, ME · On-site

$26 - $35.10/hr

Must possess Bachelor's degree in Biomedical Engineering, Biotechnology, Bioinformatics, or related ... Oversee and participate in the design, fabrication, operation, application and installation of new ...

... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ... What to Expect Next A Medpace team member will review your application and if your profile matches ...

BioMed Engineer I

Lewiston, ME · On-site

$26 - $35.10/hr

Must possess Bachelor's degree in Biomedical Engineering, Biotechnology, Bioinformatics, or related ... Oversee and participate in the design, fabrication, operation, application and installation of new ...

$124K - $186K/yr

Proven success in biotech, medical, or pharmaceutical sales in competitive environments, including ... This posting will be available for application until at least 06/09/2026. #LI-US Location: United ...

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Showing results 1-20

Biotech Application information

What is the difference between Biotech Application vs Biotech Laboratory Technician?

AspectBiotech ApplicationBiotech Laboratory Technician
Required CredentialsBachelor's degree in biotech, biology, or related field; certifications varyAssociate's or bachelor's degree in biotech, biology, or related field; certifications may be required
Work EnvironmentOffice settings, client interactions, project managementLaboratory settings, hands-on experiments, sample analysis
Employer & Industry UsagePharmaceutical companies, biotech firms, research organizationsResearch labs, biotech companies, healthcare facilities

Biotech Application roles focus on applying biotech knowledge to develop products, manage projects, and liaise with clients, often involving office work. In contrast, Biotech Laboratory Technicians perform hands-on lab work, conducting experiments and analyzing samples. Both roles require related educational backgrounds but differ mainly in work environment and daily tasks.

What are popular job titles related to Biotech Application jobs in Maine?

For Biotech Application jobs in Maine, the most frequently searched job titles are:

What job categories do people searching Biotech Application jobs in Maine look for?

The top searched job categories for Biotech Application jobs in Maine are:

Infographic showing various Biotech Application job openings in Maine as of August 2026, with employment types broken down into 81% Full Time, 14% Part Time, and 5% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Associate Clinical Trial Manager - PhD/Post-Doc (Oncology)

Medpace, Inc.

Bristol, ME • On-site, Remote

$34 - $46.50/hr

Full-time

Medical, Retirement, PTO

Re-posted 23 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research


Job description

Job Summary

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Seoul, South Korea office.  The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities.  Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities
  • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
  • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
  • Compile and maintain project-specific status reports within the clinical trial management system;
  • Interact with the internal project team, Sponsor, study sites, and third-party vendors;
  • Provide oversight and quality control of our internal regulatory filing system;
  • Provide oversight and management of study supplies;
  • Create and maintain project timelines; and
  • Coordinate project meetings and produce quality minutes.
Qualifications
  • PhD in Life Sciences;
  • Fluency in English with solid presentation skills;
  • Ability to work in a fast-paced dynamic industry within an international team;
  • Prior experience within the CRO or pharmaceutical industry not required but will be advantageous; and
  • Excellent computer (word-processing, databases, Excel, Windows), organisational, and communication skills.
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 

Please note benefits may vary based on country. 

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

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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