Qualifications MD, PhD, or PharmD: 0 to 3 years with industry experience in clinical development and bioequivalence (BE) clinical trial management or similar experience in university, hospital or ...
Qualifications MD, PhD, or PharmD: 0 to 3 years with industry experience in clinical development and bioequivalence (BE) clinical trial management or similar experience in university, hospital or ...
Plans bioequivalence studies on drug product and evaluates the bioequivalence data to recommend changes in formulation, if needed Maintains appropriate documentation of primary data records, report ...
Plans bioequivalence studies on drug product and evaluates the bioequivalence data to recommend changes in formulation, if needed Maintains appropriate documentation of primary data records, report ...
The Manager partners closely with Research & Development, Analytical Development, Manufacturing, Quality, Clinical/Bioequivalence, Supply Chain, Project Management, and external development and ...
The Manager partners closely with Research & Development, Analytical Development, Manufacturing, Quality, Clinical/Bioequivalence, Supply Chain, Project Management, and external development and ...
Biochemist
$69K - $73K/yr
Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution * Perform ...
Biochemist
$69K - $73K/yr
Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution * Perform ...
Biochemist
Chantilly, VA · On-site
Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution * Perform ...
Quick apply
Biochemist
Chantilly, VA · On-site
Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution * Perform ...
Biochemist
Chantilly, VA · On-site
$69K - $73K/yr
Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution * Perform ...
Biochemist
Chantilly, VA · On-site
$69K - $73K/yr
Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution * Perform ...
Supports design and execution of Ph1 clinical pharmacology studies (i.e FIH, relative bioavailability, bioequivalence, hepatic impairment, renal impairment, etc) * Author and provide technical input ...
Supports design and execution of Ph1 clinical pharmacology studies (i.e FIH, relative bioavailability, bioequivalence, hepatic impairment, renal impairment, etc) * Author and provide technical input ...
Scientist
Morgantown, WV · On-site
Develop and validate analytical methods to quantify drugs and metabolites in biological matrices to support bioequivalence and other pharmacokinetics studies with supervision. * Document laboratory ...
Scientist
Morgantown, WV · On-site
Develop and validate analytical methods to quantify drugs and metabolites in biological matrices to support bioequivalence and other pharmacokinetics studies with supervision. * Document laboratory ...
Develop and validate analytical methods to quantify drugs and metabolites in biological matrices to support bioequivalence and other pharmacokinetics studies with supervision. * Document laboratory ...
Develop and validate analytical methods to quantify drugs and metabolites in biological matrices to support bioequivalence and other pharmacokinetics studies with supervision. * Document laboratory ...
Oversee development activities including formulation, analytical development, bioequivalence studies, ANDA submission, and lifecycle management. * Develop, manage, and track project budgets; monitor ...
Oversee development activities including formulation, analytical development, bioequivalence studies, ANDA submission, and lifecycle management. * Develop, manage, and track project budgets; monitor ...
$16.50 - $22.25/hr
... bioequivalence approaches. In addition, the Durham facility supports development of transdermal delivery systems, nasal sprays, and other complex dosage forms, positioning the NC footprint as a ...
$16.50 - $22.25/hr
... bioequivalence approaches. In addition, the Durham facility supports development of transdermal delivery systems, nasal sprays, and other complex dosage forms, positioning the NC footprint as a ...
Senior Director, Clinical Pharmacology
New York, NY · On-site
$285K - $305K/yr
Plan, design, oversee, and interpret clinical pharmacology studies, including first-in-human, relative bioavailability/bioequivalence, food-effect, QT, drug-drug interaction, and organ impairment ...
Senior Director, Clinical Pharmacology
New York, NY · On-site
$285K - $305K/yr
Plan, design, oversee, and interpret clinical pharmacology studies, including first-in-human, relative bioavailability/bioequivalence, food-effect, QT, drug-drug interaction, and organ impairment ...
Vice President, Translational Medicine & Clinical Pharmacology
South San Francisco, CA · On-site +1
$306K - $365K/yr
... bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. * Oversee drug metabolism, pharmacokinetics, bioanalysis, and related DMPK activities supporting drug ...
Quick apply
Vice President, Translational Medicine & Clinical Pharmacology
South San Francisco, CA · On-site +1
$306K - $365K/yr
... bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. * Oversee drug metabolism, pharmacokinetics, bioanalysis, and related DMPK activities supporting drug ...
Advisor, Pharmaceutical Regulatory Systems Development
Washington, DC · On-site
$131K - $131K/yr
Specialized expertise in bioavailability and bioequivalence assessment and medicines quality control laboratories. * Strong program and project management skills, including budget planning ...
Advisor, Pharmaceutical Regulatory Systems Development
Washington, DC · On-site
$131K - $131K/yr
Specialized expertise in bioavailability and bioequivalence assessment and medicines quality control laboratories. * Strong program and project management skills, including budget planning ...
Vice President, Translational Medicine & Clinical Pharmacology
South San Francisco, CA · On-site
$306K - $365K/yr
... bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. * Oversee drug metabolism, pharmacokinetics, bioanalysis, and related DMPK activities supporting drug ...
Vice President, Translational Medicine & Clinical Pharmacology
South San Francisco, CA · On-site
$306K - $365K/yr
... bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. * Oversee drug metabolism, pharmacokinetics, bioanalysis, and related DMPK activities supporting drug ...
Conducts wide range of GLP, regulated Bioanalysis/Bioequivalence/Vaccine Clinical Assay audits in accordance with QA risk-based processes. regulations/guidelines, as well as our Company policies ...
Conducts wide range of GLP, regulated Bioanalysis/Bioequivalence/Vaccine Clinical Assay audits in accordance with QA risk-based processes. regulations/guidelines, as well as our Company policies ...
Vice President, Translational Medicine & Clinical Pharmacology
South San Francisco, CA · On-site +1
$306K - $365K/yr
... bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. * Oversee drug metabolism, pharmacokinetics, bioanalysis, and related DMPK activities supporting drug ...
Vice President, Translational Medicine & Clinical Pharmacology
South San Francisco, CA · On-site +1
$306K - $365K/yr
... bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. * Oversee drug metabolism, pharmacokinetics, bioanalysis, and related DMPK activities supporting drug ...
Senior Director, Global Programs (Regulatory and Laboratory)
Rockville, MD · On-site
$208K - $262K/yr
... Bioequivalence/Bioavailability (BE/BA) trials. * Be a thought partner to other leaders within the GHMS team as we collectively advance USP's mission and broader strategic goals. * Other duties as ...
Senior Director, Global Programs (Regulatory and Laboratory)
Rockville, MD · On-site
$208K - $262K/yr
... Bioequivalence/Bioavailability (BE/BA) trials. * Be a thought partner to other leaders within the GHMS team as we collectively advance USP's mission and broader strategic goals. * Other duties as ...
... Bioequivalence/Bioavailability (BE/BA) trials. * Be a thought partner to other leaders within the GHMS team as we collectively advance USP's mission and broader strategic goals. * Other duties as ...
... Bioequivalence/Bioavailability (BE/BA) trials. * Be a thought partner to other leaders within the GHMS team as we collectively advance USP's mission and broader strategic goals. * Other duties as ...
Analytical Laboratory Manager
Mooresville, NC · On-site
The position oversees the testing of pre-commercial release samples or for bioequivalence studies (BE) in accordance with cGMPs, GLPs, and SOPs. Essential Duties and Responsibilities * Plan and ...
Analytical Laboratory Manager
Mooresville, NC · On-site
The position oversees the testing of pre-commercial release samples or for bioequivalence studies (BE) in accordance with cGMPs, GLPs, and SOPs. Essential Duties and Responsibilities * Plan and ...
bioequivalence information
See salary details
$11K - $25.1K
0% of jobs
$25.1K - $39.2K
0% of jobs
$39.2K - $53.3K
0% of jobs
$53.3K - $67.4K
0% of jobs
$67.4K - $81.5K
0% of jobs
$81.5K - $95.5K
0% of jobs
$95.5K - $109.6K
0% of jobs
$115.2K is the 25th percentile. Wages below this are outliers.
$109.6K - $123.7K
63% of jobs
$137.2K is the 75th percentile. Wages above this are outliers.
$123.7K - $137.8K
12% of jobs
$137.8K - $151.9K
12% of jobs
$151.9K - $166K
12% of jobs
$11K
$127.2K
$166K
How much do bioequivalence jobs pay per year?
What is bioequivalence?
A Bioequivalence job typically involves conducting studies to compare the pharmacokinetics of generic drugs with their brand-name counterparts. Professionals in this field analyze drug absorption, distribution, metabolism, and excretion to ensure therapeutic equivalence. They work in pharmaceutical companies, contract research organizations (CROs), or regulatory agencies. Responsibilities may include designing and overseeing clinical trials, analyzing data, and preparing regulatory submissions. The goal is to demonstrate that the generic drug performs similarly to the branded version in terms of efficacy and safety.
What does a typical day look like for someone working in bioequivalence studies?
A typical day in bioequivalence involves designing and overseeing laboratory experiments, analyzing pharmacokinetic data, preparing reports, and ensuring that studies meet regulatory guidelines. You will often collaborate with clinical teams, statisticians, and quality assurance professionals to ensure the accuracy and validity of study results. Regular tasks may also include troubleshooting analytical equipment and participating in meetings to discuss project timelines and regulatory updates. This dynamic environment offers opportunities for continuous learning and close teamwork with other scientific professionals.
What are the key skills and qualifications needed to thrive in bioequivalence?
To thrive in a Bioequivalence Scientist role, you need a solid background in pharmaceutical sciences, analytical chemistry, or a related field, often supported by a relevant degree or certification. Familiarity with laboratory instrumentation such as HPLC/LC-MS, statistical analysis software, and regulatory guidelines (e.g., FDA or EMA) is crucial. Strong attention to detail, problem-solving abilities, and clear communication skills are highly valued. These competencies are essential to ensure accurate data analysis, regulatory compliance, and effective collaboration within cross-functional teams.
What are the most commonly searched types of Bioequivalence jobs?
The most popular types of Bioequivalence jobs are:
What job categories do people searching Bioequivalence jobs look for?
The top searched job categories for Bioequivalence jobs are:

Clinical Research Scientist
Madison, NJ
$60/hr
Contractor
Re-posted 2 days ago
Job description
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.Â
MD, PhD, or PharmD: 0 to 3 years with industry experience in clinical development and bioequivalence (BE) clinical trial management or similar experience in university, hospital or research organization
MS: 3 to 5 years of clinical development/clinical trial management
BS: 5 to 8 years with industrial or CRO clinical experience
Experience in writing clinical portions of regulatory dossiers highly preferred
Knowledge of drug development (all clinical research process including protocol and case report form design, etc)
Knowledge of GCP/ICH guidelines and FDA regulations
$60/hr
12 MONTHS
About Global Channel Management
Sourced by ZipRecruiter
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.
Industry
Recruiting and staffing services
Company size
11 - 50 Employees
Headquarters location
Austell, GA, US