9,145 Clinical Research Scientist jobs in the United States

Our client is a cutting-edge pharmaceutical company seeking a highly motivated and experienced Clinical Research Scientist to join their innovative team, operating in a fully remote capacity. This role is critical in driving the design, execution, and interpretation of clinical trials to advance novel therapies. The ideal candidate will possess a strong scientific background, a deep understanding of clinical research methodologies, and a passion for drug development. You will be responsible for contributing to the development of clinical trial protocols, overseeing study conduct, and ensuring compliance with regulatory guidelines (e.g., FDA, EMA). Key responsibilities include analyzing study data, preparing clinical study reports, and collaborating with cross-functional teams, including biostatistics, data management, and regulatory affairs. Experience in a specific therapeutic area (e.g., oncology, cardiology, neurology) is highly desirable. You will also play a key role in interacting with investigators, site staff, and external experts. A Ph.D. or Master's degree in a life science discipline (e.g., Biology, Pharmacology, Medicine) is required, along with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry. Excellent written and verbal communication skills, strong analytical abilities, and proficiency in statistical software and data analysis tools are essential. The ability to work independently, manage multiple projects concurrently, and contribute to a collaborative research environment in a remote setting is paramount. If you are a dedicated scientist eager to make a significant contribution to global health through pioneering pharmaceutical research, this is an exceptional opportunity. You will be instrumental in bringing life-changing treatments to patients.

Our client is looking for a highly skilled Clinical Research Scientist to join their innovative pharmaceutical research team in New York City, New York . This role requires hands-on involvement in the design, execution, and analysis of clinical trials. You will be responsible for developing study protocols, managing data integrity, interpreting results, and ensuring compliance with regulatory guidelines (FDA, EMA, etc.). The ideal candidate will possess a strong scientific background, extensive knowledge of clinical trial methodologies, and a proven ability to contribute to the drug development process. This position demands meticulous attention to detail, excellent analytical and statistical skills, and the capacity to work effectively within a cross-functional team of medical experts, statisticians, and regulatory affairs professionals. You will play a critical role in advancing groundbreaking therapies from preclinical stages through to market approval. This role is primarily lab and office-based, requiring your presence on-site in New York City, New York to collaborate closely with research teams and oversee experimental procedures. Strong written and verbal communication skills are essential for disseminating research findings through reports, publications, and presentations.
Responsibilities:

• Design and develop clinical trial protocols in alignment with research objectives and regulatory requirements.
• Oversee the day-to-day operations of clinical trials, ensuring data accuracy and completeness.
• Analyze clinical trial data and interpret study outcomes.
• Prepare comprehensive reports on study findings for internal review and regulatory submissions.
• Collaborate with investigators, site personnel, and cross-functional teams to ensure successful trial execution.
• Ensure all clinical trial activities adhere to Good Clinical Practice (GCP) and other relevant regulations.
• Contribute to the scientific strategy and literature review for ongoing and future research projects.
• Present research findings at scientific meetings and contribute to publications.

Qualifications:

• Ph.D. or M.D. in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine).
• Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
• In-depth understanding of clinical trial design, execution, and data analysis.
• Proficiency in statistical analysis software (e.g., SAS, R) and clinical data management systems.
• Knowledge of regulatory guidelines (e.g., FDA, ICH, GCP).
• Excellent scientific writing and presentation skills.
• Strong problem-solving and critical thinking abilities.
• Ability to work collaboratively in a team environment.

This is an exciting opportunity to contribute to life-saving research in a leading pharmaceutical organization.

Our client is looking for a highly skilled and dedicated Clinical Research Scientist to contribute to groundbreaking pharmaceutical research in Oklahoma City, Oklahoma, US . This role is integral to the design, execution, and analysis of clinical trials, advancing the development of novel therapeutics. The successful candidate will be responsible for developing study protocols, managing data integrity, interpreting clinical data, and preparing regulatory submissions. You will collaborate closely with principal investigators, clinical research associates, biostatisticians, and regulatory affairs specialists to ensure the successful and compliant execution of clinical studies. Key responsibilities include literature reviews, identifying research opportunities, designing study endpoints, and analyzing study results to assess efficacy and safety. The ideal candidate will possess a Ph.D. or Master's degree in a relevant life science discipline (e.g., pharmacology, biology, medicine) and have a minimum of 4 years of experience in clinical research within the pharmaceutical or biotechnology industry. Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., FDA, EMA) is essential. Excellent analytical, written, and verbal communication skills are required, along with the ability to work independently and as part of a multidisciplinary team. Experience with statistical analysis software and clinical data management systems is a significant advantage. This is an exciting opportunity to make a significant impact on patient care through innovative drug development.

A pioneering pharmaceutical company is seeking an experienced Clinical Research Scientist to join their innovative R&D department in Des Moines, Iowa, US . This role offers a hybrid work environment, balancing essential lab and in-office work with remote responsibilities. The Clinical Research Scientist will be instrumental in designing, implementing, and managing clinical trials for novel therapeutic agents. Key responsibilities include developing clinical trial protocols, overseeing study execution, analyzing clinical data, and interpreting results in alignment with regulatory guidelines. You will collaborate closely with cross-functional teams, including statisticians, data managers, medical writers, and regulatory affairs specialists, to ensure the successful and timely completion of clinical studies. A strong understanding of drug development processes, clinical trial methodologies, and regulatory requirements (FDA, EMA) is essential. Experience with biostatistics and data analysis is required. The ideal candidate will possess excellent scientific acumen, strong critical thinking skills, and the ability to manage multiple complex projects simultaneously. A Ph.D. or Master's degree in a relevant life science discipline (e.g., Pharmacology, Biochemistry, Medicine) is required, along with a minimum of 3-5 years of direct experience in clinical research within the pharmaceutical or biotech industry. Excellent written and verbal communication skills are necessary to effectively present scientific findings and collaborate with internal and external stakeholders. This is a compelling opportunity to contribute to life-changing medical advancements.

Our client, a leading biopharmaceutical company dedicated to advancing human health, is seeking a highly motivated and experienced Clinical Research Scientist to join their esteemed team in Seattle, Washington, US . This critical role involves the design, execution, and interpretation of clinical trials, contributing to the development of groundbreaking therapies. You will work at the forefront of medical innovation, collaborating with internal teams and external investigators to ensure the highest standards of scientific rigor and patient safety. The ideal candidate will possess a strong background in clinical research methodologies, excellent analytical skills, and a passion for translating scientific discoveries into tangible patient benefits. You will be involved in all phases of clinical development, from protocol design to data analysis and regulatory submissions.

Key Responsibilities:

• Design and develop clinical trial protocols in alignment with scientific objectives and regulatory requirements.
• Oversee the operational execution of clinical trials, ensuring adherence to Good Clinical Practice (GCP) and internal SOPs.
• Analyze and interpret clinical trial data, contributing to study reports and publications.
• Collaborate with cross-functional teams, including regulatory affairs, biostatistics, data management, and clinical operations.
• Serve as a scientific liaison with investigators, site staff, and external experts.
• Contribute to the preparation of regulatory submissions, such as Investigational New Drug (IND) applications and New Drug Applications (NDAs).
• Evaluate emerging scientific literature and technologies relevant to therapeutic areas of interest.
• Manage budgets and timelines for clinical research projects.
• Present research findings at scientific meetings and conferences.
• Ensure ethical conduct of research and protection of patient rights and safety.

Qualifications:

• Advanced degree (Ph.D., M.D., Pharm.D.) in a life science, medical, or related field.
• Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical or biotechnology industry.
• Proven experience in clinical trial design, execution, and data analysis.
• In-depth knowledge of GCP, regulatory guidelines (FDA, EMA), and clinical development processes.
• Strong scientific and medical understanding of relevant therapeutic areas.
• Excellent written and verbal communication skills, including presentation abilities.
• Proficiency in statistical analysis concepts and interpretation of clinical data.
• Ability to work effectively in a collaborative, fast-paced environment.

This position requires a dedicated professional committed to making a significant impact on patient care and advancing medical science. The role is based in Seattle, Washington, US .

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Principal Clinical Research Scientist**
**About Abbott**
Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology. In Abbott's Electrophysiology (EP) business, we're advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of.
+ Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
+ An excellent retirement savings plan with high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
This position works out of our St Paul or Plymouth, MN, Austin, TX, or Santa Clara, CA location, supporting our Electrophysiology medical device division. The **Principle Clinical Research Scientist** will lead scientific activities associated with the design, conduct, and reporting of clinical trials for this therapeutic area.
This position will participate in the development of clinical evidence to establish feasibility, achieve regulatory approvals, meet ongoing regulatory requirements, gain reimbursement, and support full commercial adoption of medical devices. You will support the analysis and interpretation of scientific data and write clinical study protocols, reports, and scientific publications. You will aid in the production of additional study-level documents including informed consent forms, case report forms, and investigator brochures. In this role, you will interact with physician Key Opinion Leaders and various cross-functional teams, including Marketing, R&D, Field Operations, Risk Management, Reimbursement, Medical Affairs, Quality, and Regulatory Affairs. You will also interact with global regulatory agencies to obtain market approval of new products, and with study sites to respond to questions throughout the study.
**What You'll Work On**
+ Develops, writes or mentors others in clinical trial design, protocol development, and publication planning.
+ Develops, writes or mentors others in generating and executing on study-level publication projects.
+ Develops, writes, or mentors others in generation of study-related documents and/or contribute content and oversight of such documents, including, but not limited to, clinical study reports, clinical study protocols, case report forms, investigational brochures, and informed consent forms.
+ Review and critically analyze statistical analysis plans.
+ Support regulatory submissions.
+ Facilitate communication between Sales and Marketing, R&D, Program Management, Reimbursement, Medical Affairs, Risk Management, Quality and Regulatory Affairs, and investigational sites.
+ Oversee study Steering Committees and Publication Committees, consisting of physician Key Opinion Leaders globally.
+ Present clinical study results to senior leaders and at investigator meetings.
+ Participate in and support audits.
**Required Qualifications**
+ Advanced degree in the sciences, medicine, or similar discipline.
+ 5+ years of clinical science experience post-degree.
+ Demonstrated scientific writing ability.
+ Experience with international medical device regulations and submissions.
+ Ability to plan and organize project assignments of substantial variety and complexity.
+ Ability to be innovative, resourceful, and work with minimal direction.
+ Excellent organization, problem solving, and communication skills and the ability to work effectively with cross-functional teams.
+ Ability to work within a team in a fast-paced, changing environment.
+ Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
+ Strong organizational and follow-up skills, as well as attention to detail.
+ Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.
**Preferred Qualifications**
+ PhD degree in the sciences, medicine, or similar discipline preferred.
+ Experience in the medical device industry.
+ Familiarity with relevant international regulatory requirements for medical devices including Quality Systems standards and clinical investigations.
+ Experience working in a quality system environment preferred.
Apply Now ( Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
**Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is $97,300.00 - $194,700.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Our client, a leading pharmaceutical innovator, is seeking a highly skilled and experienced Principal Clinical Research Scientist to contribute to groundbreaking drug development efforts in San Antonio, Texas . This senior role offers a unique opportunity to lead critical research initiatives and drive the translation of scientific discoveries into life-saving therapies. In this hybrid position, you will balance focused remote research and data analysis with essential on-site laboratory work and team collaborations. You will be responsible for designing, executing, and interpreting complex clinical studies, ensuring adherence to regulatory guidelines (e.g., FDA, EMA) and ethical principles. The ideal candidate will possess extensive expertise in a specific therapeutic area, coupled with a strong understanding of preclinical and clinical development pathways. Key responsibilities include developing study protocols, selecting appropriate research methodologies, analyzing and reporting study results, and contributing to regulatory submissions. You will collaborate closely with cross-functional teams, including statisticians, clinicians, regulatory affairs specialists, and project managers, to ensure the successful progression of research projects. Mentoring junior scientists and contributing to the scientific strategy of the organization are integral aspects of this role. A PhD in a relevant life science discipline (e.g., pharmacology, molecular biology, biochemistry) with a proven track record of successful clinical research and publications is required. Excellent communication, presentation, and problem-solving skills are essential. The ability to critically evaluate scientific literature, identify novel research opportunities, and effectively communicate complex scientific information to diverse audiences is crucial. This position demands a rigorous scientific approach, a commitment to innovation, and the ability to thrive in a fast-paced, collaborative research environment. The successful candidate will be passionate about advancing medical science and improving patient outcomes through cutting-edge pharmaceutical research.

Our client, a dynamic and innovative pharmaceutical company dedicated to advancing patient care through cutting-edge research, is looking for a highly experienced Senior Clinical Research Scientist. This critical role will contribute significantly to the design, execution, and interpretation of clinical trials across various therapeutic areas. The ideal candidate will possess a strong scientific background, deep understanding of clinical trial methodologies, and a commitment to rigorous data analysis and reporting. You will play a key role in advancing our drug candidates through the development pipeline.

Responsibilities:

• Design clinical trial protocols, including study objectives, endpoints, methodology, statistical considerations, and safety monitoring plans.
• Develop clinical study reports (CSRs), manuscripts for publication, and other scientific documents.
• Collaborate with cross-functional teams, including medical affairs, biostatistics, data management, regulatory affairs, and clinical operations.
• Provide scientific and medical expertise throughout the clinical trial process.
• Analyze and interpret clinical trial data, ensuring data integrity and accuracy.
• Stay abreast of the latest scientific literature, clinical trial advancements, and regulatory guidelines.
• Support regulatory submissions by providing scientific input and data interpretation.
• Contribute to the development of clinical development strategies for new drug candidates.
• Present study results and scientific findings at internal meetings and external conferences.
• Mentor junior research scientists and contribute to team development.

Qualifications:

• Ph.D. or M.D. in a relevant life science or medical discipline.
• Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
• Proven experience in clinical trial design and protocol development.
• Strong understanding of clinical trial methodologies, statistical principles, and data analysis.
• In-depth knowledge of regulatory requirements (FDA, ICH) relevant to clinical trials.
• Excellent scientific writing and communication skills.
• Ability to critically evaluate scientific data and translate it into actionable insights.
• Strong analytical and problem-solving skills.
• Ability to work effectively in a collaborative, multidisciplinary team environment.
• Experience in specific therapeutic areas relevant to the company's pipeline is highly desirable.
• Proficiency in statistical software and data visualization tools is a plus.

This is an outstanding opportunity to contribute to significant advancements in pharmaceutical research and development. If you are a dedicated and scientifically driven individual, we encourage you to apply. The role is located in Durham, North Carolina, US .

Our client is searching for a highly accomplished and innovative Lead Clinical Research Scientist to spearhead groundbreaking research initiatives in **Huntsville, Alabama, US**. This senior position offers a unique opportunity to contribute to the development of novel pharmaceuticals, from early-stage research through to clinical trials. The successful candidate will lead a team of dedicated scientists, guiding experimental design, data analysis, and interpretation to advance our drug discovery pipeline. Responsibilities include designing and overseeing complex preclinical and clinical studies, ensuring adherence to regulatory guidelines (FDA, EMA, etc.), and authoring comprehensive study protocols and reports. You will collaborate closely with cross-functional teams, including pharmacology, toxicology, regulatory affairs, and medical affairs, to achieve project milestones. A key aspect of this role involves staying at the forefront of scientific literature, identifying new research opportunities, and developing innovative approaches to address unmet medical needs. The Lead Clinical Research Scientist will also be instrumental in preparing scientific publications, presenting findings at international conferences, and contributing to patent applications. This position demands exceptional analytical skills, a rigorous scientific approach, and a proven track record of successfully managing research projects from concept to completion. Expertise in specific therapeutic areas relevant to our portfolio is highly desirable. You will mentor junior scientists, foster a collaborative research environment, and drive scientific excellence within the organization. This role is based in our state-of-the-art facility in Huntsville, Alabama, US , and requires full-time dedication to on-site laboratory work and team leadership. We are committed to pushing the boundaries of pharmaceutical innovation and seek individuals who share our passion for improving patient lives through cutting-edge science. Your contributions will directly impact the trajectory of new therapies, making this a deeply rewarding career opportunity. The ability to critically evaluate scientific data, troubleshoot experimental challenges, and communicate complex scientific concepts clearly to both scientific and non-scientific audiences is essential.

Responsibilities:

• Design, implement, and manage preclinical and clinical research studies.
• Lead and mentor a team of research scientists and technicians.
• Analyze and interpret complex scientific data, drawing sound conclusions.
• Author study protocols, clinical study reports, and regulatory submission documents.
• Collaborate with internal and external stakeholders, including CROs and academic institutions.
• Ensure all research activities comply with Good Clinical Practice (GCP) and relevant regulations.
• Stay current with scientific advancements and identify new research opportunities.
• Present research findings at scientific conferences and in peer-reviewed publications.
• Contribute to the development of intellectual property and patent applications.
• Manage research budgets and resources effectively.

Qualifications:

• Ph.D. in a relevant life science discipline (e.g., Pharmacology, Biochemistry, Molecular Biology).
• Minimum of 8 years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
• Demonstrated experience in clinical trial design, execution, and data analysis.
• Proven leadership experience managing research teams.
• Expertise in specific therapeutic areas (e.g., oncology, immunology, neuroscience) is a plus.
• Strong understanding of regulatory requirements (FDA, EMA) for drug development.
• Excellent analytical, problem-solving, and critical thinking skills.
• Exceptional written and verbal communication abilities.
• Proficiency with relevant scientific software and data analysis tools.
• Record of publications in high-impact scientific journals.