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No Experience Biotech Jobs in Decatur, IN (NOW HIRING)

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No Experience Biotech information

See Decatur, IN salary details

$12

$29

$49

How much do no experience biotech jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for no experience biotech in Decatur, IN is $29.10, according to ZipRecruiter salary data. Most workers in this role earn between $23.65 and $31.06 per hour, depending on experience, location, and employer.

What is a no experience biotech job?

A No Experience Biotech job is an entry-level position in the biotechnology industry that does not require prior work experience. These roles often focus on laboratory support, quality control, manufacturing, or research assistance. Employers typically seek candidates with a background in biology, chemistry, or related fields, along with a willingness to learn. Training is usually provided on the job to help employees develop essential skills. These positions can be a great starting point for building a career in biotechnology.

What kind of tasks can I expect in a no experience biotech position?

In an entry-level biotech role for candidates with no prior experience, you will typically assist with routine laboratory tasks such as preparing samples, maintaining equipment, and recording data under the supervision of experienced team members. You may also be involved in supporting quality control processes, organizing inventory, or helping with simple experiments. These responsibilities provide valuable hands-on experience with industry protocols and tools, while allowing you to learn directly from professionals in the field. Many employers offer on-the-job training and mentorship to help you build confidence and develop essential skills. Over time, you can take on more advanced duties as you demonstrate your abilities and initiative.

What are the key skills and qualifications needed to thrive in a no experience biotech position?

To thrive in a no-experience biotech role, candidates should possess a foundational understanding of biology or life sciences, strong attention to detail, and a willingness to learn on the job, often demonstrated by a relevant degree or coursework. Familiarity with basic laboratory equipment, Microsoft Office, and adherence to safety protocols are commonly expected, though training is typically provided. Strong communication, teamwork, and adaptability help individuals excel and integrate into the collaborative nature of biotech environments. These attributes are important for ensuring accuracy, safety, and professional growth in a highly regulated and rapidly evolving industry.

How to get into biotech with no experience?

To enter biotech with no experience, focus on gaining relevant skills through online courses or certifications in areas like laboratory techniques or biology. Seek entry-level positions such as lab assistant or technician, and consider internships or volunteering to build practical experience and industry connections.

How to get work experience in biotech?

To gain work experience in biotech, entry-level roles such as laboratory assistant or research technician are common starting points. Gaining relevant skills through internships, volunteering, or certifications in laboratory techniques and biotech tools can improve employability. Building a strong foundation in biology, chemistry, and data analysis is also beneficial.

What cities near Decatur, IN are hiring for No Experience Biotech jobs?

Cities near Decatur, IN with the most No Experience Biotech job openings:

No Experience Biotech jobs near you
Infographic showing various No Experience Biotech job openings in Decatur, IN as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 22% Part Time, and 5% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $60,530 per year, or $29.1 per hour.

Research Clinical Assistant

American Oncology Network

Fort Wayne, IN • On-site

$17.93 - $29.89/hr

Full-time

Posted 20 days ago

Key responsibilities

  • Supports the clinical research department by performing administrative and clerical tasks.

  • Ensures accurate and timely collection, preparation, and submission of study assessments and samples such as radiology, pathology, laboratory, and EKG data.

  • Supports ongoing clinical trial operations, including monitoring, quality audits, and maintaining regulatory and study documentation.

American Oncology Network rating

6.7

Company rating: 6.7 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

533rd of 898 rated healthcare providers

Job description

Location:

Fort Wayne Medical Oncology and Hematology

Pay Range:

$17.93 - $29.89Job Description Summary:

Responsible for various support tasks for the clinical research department. Provides administrative and clerical support to the clinical research team.

Demonstrates working knowledge of all facets of role, relevant regulations, and organizational and departmental policies and procedures. Performs other duties and projects as assigned. Performs all duties in accordance with regulatory requirements and organizational policies and procedures.

Primary Key Performance Areas

KPA 1 - Maintains working knowledge of research process

  • Remains knowledgeable and demonstrates compliance with GCP/ICH guidelines, SOPs and individual protocols
  • Attend all study initiation meetings and complete ongoing GCP and protocol-based trainings
  • Manages fax and e-mail communications in a timely manner
  • Actively seeks clarification to study processes when needed

KPA 2 - Ensures accurate and timely collection and submission of centralized study assessments (radiology, pathology, laboratory, EKG)

  • Maintains inventories for all clinical trial supplies, including restock for any study that is actively enrolling or has active patients.
  • Facilitates destruction of expired or unused supplies in accordance with site policy and study protocol.
  • Prepares supplies needed for patients in advance of scheduled appointments.
  • Completes requisitions and shipping of lab samples collected and processed by the clinic
  • Supports the collection and submission of central radiology data/images per protocol and study manuals
  • Supports the collection and submission of archival tissue Per protocol and study manuals
  • Supports the collection and submission of EKG tracings per protocol and study manuals
  • Completes Source Documents, Study Documents, Logs, and Master Files to ensure quality, completeness, and accuracy

KPA 3 - Support ongoing clinical trial operations including monitoring and quality audit functions

  • Ensures that written and verbal communication with co-workers, sponsors, and other professionals in the pharmaceutical research field are collaborative and courteous
  • Maintain, update, and distribute research information and training documents to staff and investigators as instructed
  • Reviews monitor follow-up letters and ensure outstanding issues are resolved where applicable
  • Prepare and support quality audits and inspections as needed
  • Ensure that adequate and accurate records are maintained in the patient medical record and study regulatory file
Position Qualifications/Requirements

Education:.

  • High school education required
  • Some college is preferred

Certifications/Licenses:

  • Professional clinical research certification is preferred
  • Valid state Driver's License for travel to satellite offices and offsite meetings. Compliance with the company Driver Safety Operations and Motor Vehicle Records Check Policy is required.

Previous Experience:

  • 1-2 years prior research or related medical science experience preferred

Core Capabilities:

  • Analysis & Critical Thinking: Critical thinking skills including solid problem solving, analysis, decision-making, planning, time management and organizational skills. Must be detailed oriented with the ability to exercise independent judgment.
  • Interpersonal Effectiveness: Developed interpersonal skills, emotional intelligence, diplomacy, tact, conflict management, delegation skills, and diversity awareness. Ability to work effectively with sensitive and confidential material and sometimes emotionally charged matters.
  • Communication Skills: Good command of the English language. Second language is an asset but not required. Effective communication skills (oral, written, presentation), is an active listener, and effectively provides balanced feedback.
  • Customer Service & Organizational Awareness: Strong customer focus. Ability to build an engaging culture of quality, performance effectiveness and operational excellence through best practices, strong business and political acumen, collaboration and partnerships, as well as a positive employee, physician and community relations.
  • Self-Management: Effectively manages own time, conflicting priorities, self, stress, and professional development. Self-motivated and self-starter with ability work independently with limited supervision. Ability to work remotely effectively as required.
  • Must be able to work effectively in a fast-paced, multi-site environment with demonstrated ability to juggle competing priorities and demands from a variety of stakeholders and sites.
  • Computer Skills:
    • Proficiency in MS Office Word, Excel, Power Point, and Outlook required.
    • Prior experience with electronic medical records (EMR) is preferred
    • Prior experience with clinical trial data entry systems (EDC) preferred
    • Prior Clinical Trial Management Systems (CTMS) preferred.

Travel: 0%

Standard Core Workdays/Hours: Monday to Friday 8:00 AM - 5:00 PM.

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