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Biotech Clinical Research Jobs in Indiana (NOW HIRING)

Experience in life sciences or medical fields, including imaging expertise and clinical research acquired working on clinical trials at a biotech, pharmaceutical or CRO company, having a strong ...

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ...

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ...

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Biotech Clinical Research information

What is a biotech clinical research?

A Biotech Clinical Research job involves conducting and managing clinical trials to evaluate the safety and efficacy of new drugs, medical devices, or treatments developed by biotechnology companies. Professionals in this field ensure compliance with regulatory guidelines, collect and analyze clinical data, and collaborate with cross-functional teams such as scientists, medical professionals, and regulatory authorities. Their work helps bring innovative therapies to market, improving patient care and advancing medical science.

What are the key skills and qualifications needed to thrive in biotech clinical research?

To thrive in Biotech Clinical Research, you need a solid background in life sciences, clinical trial methodologies, and regulatory compliance, usually supported by a relevant degree such as biology, biochemistry, or pharmacology. Experience with data management systems, statistical analysis software, and certifications like GCP (Good Clinical Practice) are highly valued. Exceptional attention to detail, effective communication, and strong problem-solving abilities are important soft skills for success in this role. These skills ensure clinical trials are conducted accurately, ethically, and efficiently, supporting the advancement of safe and effective biotech products.

What are some common challenges faced by professionals in biotech clinical research?

Professionals in biotech clinical research often encounter challenges such as managing complex regulatory requirements, adapting to frequent protocol amendments, and coordinating among diverse teams across multiple sites. Ensuring high data quality and maintaining strict timelines can also be demanding, especially as studies progress and new discoveries emerge. However, the dynamic nature of the work offers continuous learning opportunities and the reward of contributing to groundbreaking scientific advancements. Team members typically collaborate closely with clinical monitors, project managers, and regulatory affairs specialists to ensure every aspect of the research process runs smoothly.

What does a biotech clinical research do?

A biotech clinical research professional designs, manages, and monitors clinical trials to evaluate the safety and effectiveness of new drugs or therapies. They ensure compliance with regulatory standards, collect and analyze data, and collaborate with healthcare providers and regulatory agencies throughout the development process.

What qualifications do you need to be a biotech clinical researcher?

Biotech clinical researchers typically need a bachelor's degree in a life science, such as biology, chemistry, or related fields. Many roles require experience with clinical trial protocols, data analysis, and familiarity with regulatory requirements; advanced positions may require a master's or doctoral degree. Certifications like Good Clinical Practice (GCP) training can also enhance qualifications.

What are the most commonly searched types of Biotech Clinical Research jobs in Indiana?

The most popular types of Biotech Clinical Research jobs in Indiana are:

What are popular job titles related to Biotech Clinical Research jobs in Indiana?

For Biotech Clinical Research jobs in Indiana, the most frequently searched job titles are:

Infographic showing various Biotech Clinical Research job openings in Indiana as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 18% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Imaging Specialist Manager

Amgen

Indianapolis, IN โ€ข On-site, Remote

Full-time

Posted 12 days ago


Key responsibilities

  • Plan and execute imaging operations for clinical trials globally.

  • Manage and coordinate the operational imaging strategy, including planning, risk assessment, mitigation, and execution for clinical trials.

  • Provide oversight and expertise for imaging setup, startup activities, and maintain the quality and scientific integrity of imaging-related elements in clinical trials.


Job description

Career CategoryClinicalJob Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel likeyou'repart of something bigger,it'sbecause you are. AtAmgenour shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching,manufacturingand delivering ever-better products that reachover10 million patientsworldwide.It'stime for a career you can be proud of. Join us.

IMAGING SPECIALIST MANAGER

LIVE

What you will do

In this vital role you will plan and execute imaging operations for clinical trials globally. You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up to close-out.

Responsabilities:

  • Provide oversight and expertise for imaging setup and startup activities

  • Maintain the quality and scientific integrity of imaging-related elements in clinical trials

  • Working with the Imaging Scientist Team within Clinical Biomarkers & Diagnostics to enable E2E Imaging specialist support throughout the portfolio

  • Serve as an internal subject matter expert, advising Clinical Program Operations (CPO), and other Global Development Operations (GDO) functions, on best practices, ensuring consistent standards and key lessons learned are applied across the portfolio for continuous improvement and maximum impact of the solutions

  • Build global cross-functional relationships and collaborate with clinical teams to integrate imaging into trials and update senior management

WIN

What we expectofyou

We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:

  • Experience in life sciences or medical fields, including imaging expertise and clinical research acquired working on clinical trials at a biotech, pharmaceutical or CRO company, having a strong understanding of clinical development programs in a global setting

  • Experience at or oversight of outside clinical research vendors (CRO's, central labs, imaging vendors, etc.)

  • Experience in operationalizing global clinical studies with imaging and vendor management

  • Good understanding of quality oversight and process improvement

  • Ability to network and establish relationships cross-functionally

  • Project and Program management and phenomenal communication skills

  • Degree educated

THRIVE

What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.

  • Vast opportunities to learn and move up and across our global organization

  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Location: Ability to work remotely from UK/US.

APPLY NOW

for a career that defies imagination

In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.

careers.amgen.com

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

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