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Drug Development Jobs in Florida (NOW HIRING)

Research Recruitment Assistant

Miami, FL · On-site

$16.25 - $20/hr

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a ...

File Clerk - Per Diem

Miami, FL · On-site

$15.75 - $19/hr

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a ...

Screening Deputy Lead

Miami, FL · On-site

$111K/yr

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a ...

Screening Research Technician

Miami, FL · On-site

$17.25 - $23.75/hr

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a ...

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a ...

Phlebotomist - PRN-The Villages

The Villages, FL · On-site

$15 - $18.75/hr

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve ...

Showing results 21-40

Drug Development information

See Florida salary details

$24.7K

$57.9K

$99.4K

How much do drug development jobs pay per year?

As of Sep 15, 2026, the average yearly pay for drug development in Florida is $57,869.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,700.00 and $67,600.00 per year, depending on experience, location, and employer.

What is drug development?

Drug development is the process of bringing a new pharmaceutical drug to market. It involves several stages, including drug discovery, preclinical research, clinical trials, and regulatory approval. Each stage is designed to ensure the safety, efficacy, and quality of the drug before it can be made available to patients. The entire process can take several years and requires collaboration between scientists, clinicians, regulatory agencies, and pharmaceutical companies.

What are the typical stages of collaboration between different teams in a drug development role?

In drug development, professionals regularly collaborate across multidisciplinary teams, including research scientists, clinical trial coordinators, regulatory affairs specialists, and manufacturing experts. Early stages involve close work with research and discovery teams to identify promising compounds, followed by coordination with clinical teams during trial phases, and finally with regulatory and production teams as the drug moves toward approval and commercialization. Effective communication and cross-functional teamwork are essential, as each stage relies on timely data sharing and joint problem-solving to navigate complex challenges.

What are the key skills and qualifications needed to thrive in drug development, and why are they important?

To thrive in Drug Development, you need a strong background in pharmaceutical sciences, biology, or chemistry, often supported by an advanced degree (e.g., PhD, PharmD, or MSc). Familiarity with regulatory compliance, clinical trial management systems, and data analysis software such as SAS or R is typically required. Excellent problem-solving, project management, and cross-functional communication skills help professionals excel in this multidisciplinary field. These competencies ensure that new drugs are developed safely, efficiently, and in accordance with regulatory standards.

What is the difference between Drug Development vs Pharmacologist?

AspectDrug DevelopmentPharmacologist
Required CredentialsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields; often requires experience in clinical trialsDegree in Pharmacology, Pharmacy, or related fields; may require licensing or certification for clinical practice
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial sitesResearch labs, hospitals, academic institutions, regulatory agencies
Industry UsageDeveloping new drugs, overseeing clinical trials, regulatory submissionsStudying drug effects, mechanisms, safety, and efficacy; advising on drug use

While both roles are integral to the pharmaceutical industry, Drug Development focuses on creating and bringing new drugs to market through research, testing, and regulatory processes. Pharmacologists primarily study how drugs interact with biological systems, often working in research or clinical settings to understand drug effects and safety. The two roles often collaborate but differ in their core responsibilities and career focus.

How much do drug development professionals make?

Drug development professionals, including roles such as research scientists and clinical trial managers, typically earn salaries ranging from $70,000 to over $130,000 annually, depending on experience, education, and location. Senior positions or those with specialized skills and certifications can earn higher salaries, especially in biotech and pharmaceutical companies.

Is drug development a good career?

Drug development is a challenging and rewarding career that involves research, clinical trials, and regulatory processes to bring new medications to market. It requires strong scientific knowledge, attention to detail, and often collaboration across multidisciplinary teams. The field offers opportunities for growth, innovation, and contributing to public health, but can also involve long hours and high responsibility.

What career develops drugs?

A career in drug development typically involves roles such as pharmacologist, medicinal chemist, clinical researcher, or regulatory affairs specialist. These professionals work in laboratories, research facilities, or pharmaceutical companies to discover, test, and bring new drugs to market, often requiring knowledge of biology, chemistry, and regulatory processes.

What are popular job titles related to Drug Development jobs in Florida?

For Drug Development jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Drug Development jobs?

Cities in Florida with the most Drug Development job openings:

Infographic showing various Drug Development job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $57,869 per year, or $27.8 per hour.

EMT - Paramedic Per Diem (Evening / Night)

Miami, FL • On-site

Other

Re-posted 13 days ago


Job description

Quotient Sciences: Molecule To Cure. Fast.

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing.

Our proprietary and disruptive platform – "Translational Pharmaceutics®" – integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times.

Why join us: Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.

The Role
  • Responsible for the supervision and monitoring of volunteer safety through telemetry monitoring within scope of practice
  • To collect biological samples, performs phlebotomy, vital signs and ECG's in accordance with the specific activity schedule
  • To track overall study event schedule and participant compliance
  • To comply and adhere to GCP guidelines and regulations as required of this role
  • To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards
  • To ensure subject safety at all times
Main Tasks and Responsibilities
  • Responsible for the monitoring of volunteer safety as applicable through scope of practice
  • Able to respond to medical emergency and follow medical directives within scope of practice
  • Responsible for communicating any noted adverse within scope of practice
  • Adherence to applicable SOPs and Protocol
  • Responsible for collection of biological samples; e.g. blood, urine, stool, sputum
  • Responsible for drawing blood specimens (by venipuncture) according to the times specified in the study schedules
  • Responsible for recording and maintaining records of blood draws and other biological specimen collections (per SOPs) via paper or electronic forms
  • Assist with the proper labelling and preparation of blood collection tubes when indicated
  • Assures that all necessary blood collection tubes, equipment and supplies are on the floor prior to blood draw time
  • Prepares the unit for any scheduled activities and upon completion removes all equipment and/or supplies from the floor
  • Measures and records vital signs accurately; recognizes and reports any abnormal vital signs accordingly
  • Operates ECG machine, performs ECGs, and/or works with holter monitors if trained and within scope of practice
  • Promptly reports any study participant's adverse event and/or lack of compliance to the Clinical Research Nurse
  • Must be familiar with proper phlebotomy and laboratory procedures in compliance with OSHA regulations, Good Clinical Practices and Quotient Sciences Operating Procedures
  • Responsible for proper biomedical waste disposal procedures and schedules
  • Responsible for reading and understanding all protocols and schedules
  • Responsible for assisting in the recording and distributing of meals to study participants according to strict meal schedules
  • Assures that the unit is kept clean and orderly at all times and removes any items not permitted from the floor
  • Able to interact and maintain a professional demeanour with study participants during their inpatient stay
  • Responsible for observing confidentiality practices regarding any protocols, subject information and/or any relevant industry information at all times
  • Assists with the preparation of data collection binders and study documents as assigned by the Clinical Research Nurse
  • Assists with any other duties as assigned
Job Demands

The job may involve the following:

  • Very high concentration of work
  • Strict and tight deadlines
  • Having to juggle a range of tasks/issues simultaneously
  • Working in a hazardous environment with high requirement to follow safety procedures
  • Working outside normal working hours
  • Needing to respond to client demands
The Candidate
  • Current/Valid EMT-Basic or EMT-Paramedic. If Paramedic current Advanced Cardiac Life Support (ACLS) certification
  • Minimum two years of active phlebotomy experience preferred
  • Required to have working knowledge of OSHA regulations and proper blood collection techniques (evaluable during employee orientation period)
  • Able to follow medical directives
  • High attention to details
  • Excellent communication and interpersonal skills
Application Requirements

When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.

Our Commitment to Diversity, Equity and Inclusion

Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.

Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.

This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.

Our Approach to AI in Recruitment

At Quotient Sciences, we use technology, including AI-enabled tools, to support parts of our recruitment process and help create an efficient, consistent, and inclusive candidate experience. Any use of AI is subject to human oversight, and hiring decisions are made by people, not technology.

While we embrace innovation, our recruitment process remains deeply human. Candidates who progress through our recruitment process are supported by a dedicated recruitment contact, and many of our selection processes include in-person interviews. We believe the best hiring decisions come from real conversations, giving candidates the opportunity to meet future colleagues, experience our culture and showcase their strengths beyond their application.

We recognize that candidates may choose to use AI tools when preparing applications. We encourage the responsible use of technology to support research, preparation, and drafting. However, applications should reflect your own skills, experiences, and perspectives. Throughout the recruitment process, we assess authenticity, critical thinking, technical capability, and the unique contribution you can bring to Quotient Sciences. Content generated entirely by AI may not provide an accurate representation of your suitability for the role.