7,898 Clinical Research Scientist jobs in the United States
Clinical Research Scientist
30303 Atlanta, Georgia
$110000 Annually
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Posted 3 days ago
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Job Description
Our client is looking for a highly qualified Clinical Research Scientist to contribute to groundbreaking pharmaceutical research in **Atlanta, Georgia, US**. This role operates on a hybrid model, requiring both on-site laboratory work and remote data analysis and reporting. You will be responsible for the design, execution, and interpretation of clinical studies, ensuring adherence to regulatory guidelines and scientific rigor. Key responsibilities include developing study protocols, overseeing data collection and management, analyzing research findings, and preparing scientific publications and presentations. The ideal candidate will possess a strong scientific background in a relevant discipline such as pharmacology, biology, or medicine, coupled with extensive experience in clinical trial management. You will work with cross-functional teams, including clinicians, statisticians, and regulatory affairs specialists. Proficiency in statistical analysis software (e.g., SAS, R) and a deep understanding of Good Clinical Practice (GCP) guidelines are essential. A Ph.D. or Master's degree in a life science or related field is required. A minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry is necessary. Excellent critical thinking, problem-solving, and written communication skills are crucial for success in this role. The ability to manage multiple projects concurrently and thrive in a dynamic research environment is key. This is an exceptional opportunity to advance your career in pharmaceutical research and make a meaningful impact on healthcare.
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0
Clinical Research Scientist
30303 Atlanta, Georgia
$110000 Annually
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Posted 4 days ago
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Job Description
Our client, a cutting-edge pharmaceutical company at the forefront of medical innovation, is actively seeking a highly motivated and experienced Clinical Research Scientist. This is a fully remote position, offering the flexibility to contribute to groundbreaking research from anywhere. The successful candidate will be instrumental in the design, execution, and analysis of clinical trials for novel therapeutic agents. You will be responsible for protocol development, study site selection, monitoring trial progress, and ensuring adherence to regulatory guidelines and ethical standards. The ideal candidate possesses a Ph.D. or equivalent in a relevant scientific field, with extensive experience in clinical trial management and data analysis within the pharmaceutical or biotechnology industry. Strong knowledge of GCP, FDA regulations, and statistical analysis software is essential. Key responsibilities include collaborating with cross-functional teams, including R&D, regulatory affairs, and clinical operations; preparing study reports and regulatory submissions; and presenting findings at scientific conferences. This role demands exceptional analytical, problem-solving, and communication skills, with a commitment to advancing patient care through rigorous scientific inquiry. You will have the unique opportunity to shape the future of medicine from the convenience of your home office, impacting lives globally.
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1
Clinical Research Scientist
89101 Sunrise Manor, Nevada
$120000 Annually
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Posted 5 days ago
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Job Description
Join **our client**'s pioneering pharmaceutical team as a remote Clinical Research Scientist and contribute to groundbreaking drug development. Based remotely, you will be at the forefront of designing and executing clinical trials, from protocol development to data analysis and reporting. Your expertise will be crucial in evaluating the safety and efficacy of new pharmaceutical compounds. This role requires a PhD in a relevant scientific discipline (e.g., Pharmacology, Biomedical Sciences, Medicine) and a strong background in clinical trial methodologies, regulatory affairs (FDA, EMA), and statistical analysis. You will manage the entire lifecycle of clinical studies, ensuring adherence to Good Clinical Practice (GCP) guidelines and ethical standards. Responsibilities include developing study protocols, selecting and managing clinical trial sites, overseeing data collection and monitoring, interpreting study results, and preparing regulatory submission documents. Collaboration with internal teams (R&D, regulatory affairs, clinical operations) and external partners (investigators, CROs) will be key to success. The ideal candidate demonstrates exceptional analytical, problem-solving, and communication skills, with a proven ability to lead complex research projects in a virtual setting. We seek individuals passionate about advancing medical treatments and making a tangible difference in patient lives. As a remote-first organization, we provide the tools and support for you to excel from anywhere. This position offers a competitive compensation package and excellent opportunities for professional growth within a leading pharmaceutical company. Become an integral part of our mission to improve global health.
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2
Clinical Research Scientist
84097 Cottonwood Heights, Utah
$105000 Annually
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Posted 5 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly qualified Clinical Research Scientist to contribute to groundbreaking drug development initiatives. This role involves the design, execution, and analysis of clinical trials, ensuring adherence to rigorous scientific and regulatory standards. You will be responsible for developing clinical trial protocols, managing study timelines, analyzing data, and preparing comprehensive reports. Key responsibilities include collaborating with cross-functional teams, including medical affairs, regulatory affairs, and data management, to ensure the successful progression of clinical research projects. You will also play a role in interpreting study results and contributing to the scientific literature.
The ideal candidate will possess a strong scientific background with extensive experience in clinical research methodologies and pharmaceutical development. Excellent analytical, statistical, and problem-solving skills are essential for designing robust trials and interpreting complex data sets. You should have a thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements. This role requires a detail-oriented and highly organized individual with strong written and verbal communication skills, capable of effectively communicating scientific information to diverse audiences. A commitment to scientific integrity and advancing patient care is paramount.
Responsibilities:
This position is based in Provo, Utah, US . We are looking for candidates with a Ph.D. or Master's degree in a life science, biomedical science, or a related field. A minimum of 3 years of experience in clinical research within the pharmaceutical or biotechnology industry is required. Experience in designing and managing Phase I-III clinical trials is highly desirable. Strong knowledge of statistical analysis software (e.g., SAS, R) and data visualization tools is a plus. Excellent scientific writing and presentation skills are expected.
The ideal candidate will possess a strong scientific background with extensive experience in clinical research methodologies and pharmaceutical development. Excellent analytical, statistical, and problem-solving skills are essential for designing robust trials and interpreting complex data sets. You should have a thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements. This role requires a detail-oriented and highly organized individual with strong written and verbal communication skills, capable of effectively communicating scientific information to diverse audiences. A commitment to scientific integrity and advancing patient care is paramount.
Responsibilities:
- Design and develop clinical trial protocols.
- Oversee the planning and execution of clinical studies.
- Manage study timelines and budgets effectively.
- Analyze clinical trial data and interpret study results.
- Prepare clinical study reports and regulatory submission documents.
- Collaborate with investigators, study coordinators, and clinical research associates.
- Ensure compliance with GCP guidelines and regulatory requirements.
- Contribute to the scientific strategy for drug development.
- Stay updated on scientific advancements and industry best practices.
This position is based in Provo, Utah, US . We are looking for candidates with a Ph.D. or Master's degree in a life science, biomedical science, or a related field. A minimum of 3 years of experience in clinical research within the pharmaceutical or biotechnology industry is required. Experience in designing and managing Phase I-III clinical trials is highly desirable. Strong knowledge of statistical analysis software (e.g., SAS, R) and data visualization tools is a plus. Excellent scientific writing and presentation skills are expected.
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3
Clinical Research Scientist
78205 San Antonio, Texas
$95000 Annually
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Posted 5 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking a highly skilled and dedicated Clinical Research Scientist to join their innovative team. This fully remote position is perfect for a scientist who thrives in a flexible work environment and is passionate about advancing medical research. You will play a vital role in the design, execution, and interpretation of clinical trials, contributing to the development of life-saving therapies. Your responsibilities will encompass protocol development, data analysis, regulatory submissions, and collaboration with cross-functional teams, including medical affairs, regulatory affairs, and clinical operations.
Key responsibilities include:
The ideal candidate will hold a Ph.D. or M.D. in a life sciences discipline (e.g., Biology, Pharmacology, Medicine, Biochemistry) or a Master's degree with significant relevant experience. A minimum of 3-5 years of experience in clinical research within the pharmaceutical or biotechnology industry is required. Demonstrable experience in designing and managing clinical trials is essential. Strong understanding of regulatory requirements (FDA, EMA) and Good Clinical Practice (GCP) is mandatory. Excellent written and verbal communication skills are crucial for report writing, presentations, and scientific exchange. The ability to work independently, manage multiple projects simultaneously, and collaborate effectively in a remote team setting is critical. This role offers a competitive compensation package, robust benefits, and the opportunity to contribute to groundbreaking medical advancements from a remote location. This position is based in San Antonio, Texas, US , but is performed remotely.
Key responsibilities include:
- Developing and writing clinical trial protocols, amendments, and Investigator's Brochures.
- Overseeing the conduct of clinical trials, ensuring compliance with ICH-GCP guidelines and regulatory requirements.
- Analyzing clinical trial data, interpreting results, and contributing to study reports and publications.
- Collaborating with biostatisticians and data management teams on data analysis and reporting.
- Preparing regulatory submission documents (e.g., IND, NDA) in conjunction with regulatory affairs.
- Providing scientific and clinical input to study design and operational planning.
- Engaging with key opinion leaders (KOLs) and investigators to ensure scientific integrity and patient safety.
- Monitoring study progress, identifying risks, and implementing mitigation strategies.
- Staying current with scientific literature, emerging trends, and advancements in the relevant therapeutic area.
The ideal candidate will hold a Ph.D. or M.D. in a life sciences discipline (e.g., Biology, Pharmacology, Medicine, Biochemistry) or a Master's degree with significant relevant experience. A minimum of 3-5 years of experience in clinical research within the pharmaceutical or biotechnology industry is required. Demonstrable experience in designing and managing clinical trials is essential. Strong understanding of regulatory requirements (FDA, EMA) and Good Clinical Practice (GCP) is mandatory. Excellent written and verbal communication skills are crucial for report writing, presentations, and scientific exchange. The ability to work independently, manage multiple projects simultaneously, and collaborate effectively in a remote team setting is critical. This role offers a competitive compensation package, robust benefits, and the opportunity to contribute to groundbreaking medical advancements from a remote location. This position is based in San Antonio, Texas, US , but is performed remotely.
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4
Clinical Research Scientist
35801 Huntsville, Alabama
$105000 Annually
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Posted 7 days ago
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Job Description
Our client is a pioneering pharmaceutical company seeking a highly skilled and dedicated Clinical Research Scientist to join their innovative team. This is a fully remote position, offering flexibility and the opportunity to contribute to groundbreaking medical advancements from anywhere.
As a Clinical Research Scientist, you will be responsible for the scientific and operational aspects of clinical trials, from protocol development through to study close-out. Your primary focus will be on designing and executing clinical studies that adhere to rigorous scientific principles and regulatory guidelines. This includes developing study protocols, case report forms (CRFs), and statistical analysis plans. You will work closely with internal and external stakeholders, including investigators, study coordinators, and regulatory authorities, to ensure the successful conduct of clinical trials. Monitoring study progress, analyzing data, and interpreting results to assess drug safety and efficacy will be core duties. You will also be involved in preparing clinical study reports, manuscripts for publication, and presentations for scientific conferences.
The ideal candidate will possess a PhD or Master's degree in a life science discipline such as Pharmacology, Biology, Toxicology, or a related field. A minimum of 5 years of experience in clinical research, with a focus on study design and execution within the pharmaceutical or biotechnology industry, is required. In-depth knowledge of Good Clinical Practice (GCP) guidelines, regulatory requirements (e.g., FDA, EMA), and the drug development process is essential. Strong analytical and critical thinking skills, with the ability to interpret complex scientific data, are crucial. Excellent written and verbal communication skills are necessary for protocol writing, report generation, and scientific presentations. Experience with electronic data capture (EDC) systems and statistical software is highly desirable. The ability to manage multiple projects simultaneously, prioritize tasks, and work effectively in a remote, collaborative environment is key. This role requires a passionate individual committed to advancing patient care through rigorous scientific research.
As a Clinical Research Scientist, you will be responsible for the scientific and operational aspects of clinical trials, from protocol development through to study close-out. Your primary focus will be on designing and executing clinical studies that adhere to rigorous scientific principles and regulatory guidelines. This includes developing study protocols, case report forms (CRFs), and statistical analysis plans. You will work closely with internal and external stakeholders, including investigators, study coordinators, and regulatory authorities, to ensure the successful conduct of clinical trials. Monitoring study progress, analyzing data, and interpreting results to assess drug safety and efficacy will be core duties. You will also be involved in preparing clinical study reports, manuscripts for publication, and presentations for scientific conferences.
The ideal candidate will possess a PhD or Master's degree in a life science discipline such as Pharmacology, Biology, Toxicology, or a related field. A minimum of 5 years of experience in clinical research, with a focus on study design and execution within the pharmaceutical or biotechnology industry, is required. In-depth knowledge of Good Clinical Practice (GCP) guidelines, regulatory requirements (e.g., FDA, EMA), and the drug development process is essential. Strong analytical and critical thinking skills, with the ability to interpret complex scientific data, are crucial. Excellent written and verbal communication skills are necessary for protocol writing, report generation, and scientific presentations. Experience with electronic data capture (EDC) systems and statistical software is highly desirable. The ability to manage multiple projects simultaneously, prioritize tasks, and work effectively in a remote, collaborative environment is key. This role requires a passionate individual committed to advancing patient care through rigorous scientific research.
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5
Clinical Research Scientist
78229 San Antonio, Texas
$125000 Annually
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Posted 15 days ago
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Job Description
A leading pharmaceutical research institution in **San Antonio, Texas, US** is looking for a talented and dedicated Clinical Research Scientist. This critical role supports the design, execution, and analysis of groundbreaking clinical trials aimed at developing novel therapeutic agents. The successful candidate will be instrumental in advancing our pipeline of innovative medicines. Responsibilities include developing study protocols, designing clinical trial methodologies, overseeing data collection and management, and performing statistical analysis of trial results. You will collaborate closely with investigators, study coordinators, and regulatory affairs teams to ensure the highest standards of scientific rigor and compliance with Good Clinical Practice (GCP) guidelines. The scientist will also be responsible for preparing manuscripts for publication in peer-reviewed journals and presenting findings at scientific conferences. A Ph.D. in Pharmacology, Biology, or a related life sciences discipline is a prerequisite. A minimum of 5 years of experience in clinical trial design and execution within the pharmaceutical or biotechnology industry is required. Strong knowledge of statistical analysis methods and experience with statistical software (e.g., SAS, R) are essential. Excellent written and verbal communication skills are necessary for protocol development, report writing, and scientific presentations. Experience with regulatory submissions and interactions with health authorities (e.g., FDA) is a plus. This position offers a stimulating research environment, opportunities for professional growth, and the chance to make a significant contribution to patient health. If you are a passionate scientist driven by a desire to discover and develop new treatments, this is an ideal opportunity.
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6
Clinical Research Scientist
76102 Fort Worth, Texas
$115000 Annually
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Posted 15 days ago
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Job Description
Our client, a leading pharmaceutical company at the forefront of medical innovation, is seeking a dedicated and experienced Clinical Research Scientist to join their esteemed team in Fort Worth, Texas, US . This role is instrumental in the design, execution, and analysis of clinical trials, contributing directly to the development of new life-saving therapies. You will be responsible for developing clinical trial protocols, overseeing patient recruitment and data collection, and ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. Key responsibilities include collaborating with investigators, study coordinators, and regulatory affairs teams; analyzing clinical data to evaluate drug efficacy and safety; and preparing comprehensive study reports and regulatory submissions. The Clinical Research Scientist will also stay abreast of scientific literature and emerging trends in clinical research. This position requires a strong scientific background, excellent analytical skills, and meticulous attention to detail. A Master's or Ph.D. in a life science discipline (e.g., Pharmacology, Biology, Biochemistry, Medicine) is required, along with at least 5 years of experience in clinical research, preferably within the pharmaceutical or biotechnology industry. Experience with statistical analysis software (e.g., SAS, R) and a thorough understanding of clinical trial design and regulatory affairs are essential. Join us to advance groundbreaking pharmaceutical research and make a difference in global health.
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7
Clinical Research Scientist
32801 Oakland, Florida
$110000 Annually
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Posted 15 days ago
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Job Description
Our client, a distinguished leader in pharmaceutical innovation, is seeking a highly analytical and detail-oriented Clinical Research Scientist to contribute to groundbreaking research in Orlando, Florida, US . This role is integral to the drug development lifecycle, focusing on the design, execution, and interpretation of clinical trials. The ideal candidate will possess a strong scientific background, extensive experience in clinical research methodologies, and a passion for advancing patient care through novel therapies. You will work collaboratively with cross-functional teams to ensure the integrity and success of our clinical development programs.
Primary Responsibilities:
Primary Responsibilities:
- Design and develop clinical trial protocols in alignment with regulatory guidelines and scientific objectives.
- Oversee the execution of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Monitor trial progress, analyze data, and interpret results to inform decision-making.
- Prepare clinical study reports, regulatory submissions, and scientific publications.
- Collaborate with internal teams (e.g., biostatistics, data management, regulatory affairs) and external partners (e.g., investigators, CROs).
- Contribute to the scientific strategy and development of new drug candidates.
- Ensure the safety and well-being of trial participants through rigorous monitoring and risk assessment.
- Stay abreast of the latest scientific literature, therapeutic advancements, and regulatory changes in the pharmaceutical industry.
- Provide scientific and technical expertise to study teams and stakeholders.
- Manage relationships with clinical investigators and study sites.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Pharmacology, Medicine, Biology, Biochemistry).
- Minimum of 5 years of experience in clinical research, with a significant focus on clinical trial design and management within the pharmaceutical or biotechnology industry.
- Strong understanding of clinical trial phases, regulatory requirements (FDA, EMA), and GCP guidelines.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proven ability to interpret complex scientific data and translate findings into actionable insights.
- Exceptional written and verbal communication skills, with experience in scientific writing and presentations.
- Proficiency in statistical analysis concepts and clinical data review.
- Ability to manage multiple projects concurrently in a fast-paced environment.
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8
Clinical Research Scientist
23218 Richmond, Virginia
$110000 Annually
WhatJobs
Posted 15 days ago
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Job Description
Our client is seeking an experienced Clinical Research Scientist to contribute to groundbreaking pharmaceutical research in **Richmond, Virginia, US**. This role is crucial for designing, implementing, and overseeing clinical trials, ensuring adherence to scientific protocols and regulatory guidelines. The ideal candidate will possess a strong background in clinical research methodology, data analysis, and pharmaceutical development. You will be responsible for developing clinical trial protocols, identifying investigational sites, and managing relationships with clinical investigators and study staff. Key duties include monitoring study progress, ensuring data integrity, and analyzing clinical trial results to assess drug efficacy and safety. You will also be involved in preparing regulatory submissions, scientific publications, and presentations. Experience with various therapeutic areas and knowledge of GCP (Good Clinical Practice) and FDA regulations are essential. The successful applicant will demonstrate excellent scientific acumen, critical thinking skills, and the ability to manage complex projects in a collaborative environment. This position offers a competitive salary, comprehensive benefits, and significant opportunities for professional growth within a leading pharmaceutical company located in **Richmond, Virginia, US**. Responsibilities:
- Design and develop clinical trial protocols in accordance with scientific objectives and regulatory requirements.
- Identify and qualify clinical trial sites and investigators.
- Oversee the conduct of clinical trials, ensuring compliance with GCP and study protocols.
- Manage clinical trial data, ensuring accuracy, completeness, and integrity.
- Analyze and interpret clinical trial data, preparing reports on study findings.
- Collaborate with cross-functional teams, including regulatory affairs, data management, and biostatistics.
- Prepare and submit regulatory documents to health authorities (e.g., FDA, EMA).
- Contribute to the writing of scientific publications and presentations.
- Monitor the safety and efficacy of investigational products.
- Stay abreast of scientific advancements and regulatory changes in the pharmaceutical industry.
- Ph.D. or Master's degree in a life science, pharmaceutical science, or a related field.
- Minimum of 5 years of experience in clinical research, preferably in the pharmaceutical industry.
- In-depth knowledge of clinical trial design, execution, and data analysis.
- Strong understanding of GCP, ICH guidelines, and regulatory submission processes (FDA).
- Experience with various therapeutic areas is a plus.
- Excellent scientific writing and communication skills.
- Proficiency in statistical analysis software (e.g., SAS, R) is desirable.
- Strong project management and organizational abilities.
- Ability to work independently and collaboratively in a team setting.
- Detail-oriented with a commitment to scientific rigor.
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