8,327 Clinical Research jobs in the United States

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.

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:

• 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.

Qualifications:

• 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.

This is an exciting opportunity to be at the forefront of pharmaceutical research and contribute to the development of life-changing medicines. If you are a dedicated scientist driven by innovation and patient outcomes, we encourage you to apply.

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.

Qualifications:

• 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.

At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.
Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we're working at the pace of change on diagnostic tools that address the world's biggest health challenges, driven by knowing that behind every test there is a patient waiting.
Learn about the Danaher Business System ( which makes everything possible.
The Senior Clinical Research Scientist reporting to the Director, Clinical Research, develops and independently writes clinical documentation including clinical protocols, clinical study reports and clinical justifications in support of research and new product development, registration and commercialization of products.
This position is part of Clinical Affairs and will be an Onsite Role in Sunnyvale, CA. The senior clinical research scientist will work on advanced, complex projects requiring state of the art knowledge in oncology and/or infectious disease molecular diagnostics. This is an exciting opportunity to collaborate with other Cepheid scientists, external partners, Government Affairs, Medical and Scientific Affairs on developing the product evidence strategy plan (PESP).
In this role, you will have the opportunity to:
+ Manage strategies for obtaining clinical evidence using the product evidence strategy plan process (PESP)
+ Develop strategies for clinical trials and ensure that activities are conducted in compliance with current applicable regulations, laws and guidance including but not limited to US and EU and global regulation as well as with Cepheid's policies and procedures.
+ Establish scientific methods for design and implementation of clinical protocols and have oversight for clinical strategy, protocol development and clinical study reports for US and OUS registration studies
+ Prepares scientific content of clinical study reports and review clinical and analytical sections for regulatory submissions to ensure data meets all necessary regulatory standards.
+ Review pertinent literature, prepare white papers/manuscripts, and provide education to Cepheid staff as needed.
The essential requirements of the job include:
+ Bachelor's degree in Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology with 5+ years of related work experience OR Master's degree in Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology with 3+ years of related work experience OR Doctoral degree in Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology with related work experience.
+ Experience with in vitro diagnostic (IVD) products, preferably in molecular diagnostics or immunodiagnostics, in oncology and/ or infectious disease
+ Proficiency in Microsoft Office Suite
It would be a plus if you also possess previous experience in:
+ A Masters or PhD in Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology
+ Strong scientific background with deep understanding of oncology/infectious disease and the molecular diagnostic area
+ Preferred experience in IVDD/IVDR or MDD/MDR regulations
Physical Demands:
+ Ability to travel up to 10% overnight, domestic and international
Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.
The salary range for this role is $111,100 - 152,800. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1- or .
Operating Company: Cepheid

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.
**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 **Senior Clinical Research Scientist** will lead scientific activities associated with the design, conduct, and reporting of clinical trials for this therapeutic area.
As the Senior Clinical Research Scientist, you 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**
+ Participate in clinical trial design, protocol development, and publication planning.
+ Generate and execute on study-level publication projects.
+ Prepare clinical study reports or report sections.
+ 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.
+ 4+ years of clinical research work experience post-degree.
+ Demonstrated scientific writing ability.
+ 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 and as an individual contributor 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.
**Preferred Qualifications**
+ Experience in the medical device industry.
+ Experience with international medical device regulations and submissions.
+ 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 $75,300.00 - $150,700.00. 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 is a leading pharmaceutical innovator seeking a Lead Clinical Research Scientist to drive groundbreaking studies in Chicago, Illinois, US . This pivotal role involves the design, execution, and interpretation of clinical trials for novel therapeutic agents, focusing on patient safety and data integrity. The ideal candidate will possess extensive experience in clinical trial management, a deep understanding of pharmaceutical development processes, and a passion for advancing patient care through innovative medicine.

Key Responsibilities:

• Lead the development and execution of clinical trial protocols, ensuring alignment with regulatory requirements and scientific objectives.
• Oversee the day-to-day clinical operations of assigned trials, including site selection, initiation, monitoring, and close-out.
• Collaborate with cross-functional teams, including R&D, regulatory affairs, medical affairs, and data management, to ensure seamless trial conduct.
• Develop and manage relationships with clinical investigators, site staff, and external vendors.
• Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other relevant guidelines.
• Analyze and interpret clinical data, contributing to study reports, publications, and regulatory submissions.
• Provide scientific and strategic input into the drug development process, from early-stage research to post-market studies.
• Mentor and guide junior clinical research associates and scientists.
• Prepare essential study documents, such as Investigator Brochures, informed consent forms, and case report forms.
• Monitor trial progress, identify potential risks and issues, and implement corrective actions as needed.

Qualifications:

• Advanced degree (Ph.D., Pharm.D., M.D.) in a life sciences or health-related field.
• Minimum of 8 years of experience in clinical research within the pharmaceutical or biotechnology industry.
• Proven track record in leading and managing Phase I-IV clinical trials.
• In-depth knowledge of clinical trial design, statistical principles, and data analysis.
• Strong understanding of regulatory requirements (FDA, EMA) and GCP guidelines.
• Excellent project management and organizational skills, with the ability to manage multiple projects simultaneously.
• Exceptional written and verbal communication skills, with strong presentation abilities.
• Ability to work independently and collaboratively in a fast-paced, team-oriented environment.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.

This is an outstanding opportunity to join a forward-thinking organization and make a significant impact on the development of life-saving therapies.

A leading biotechnology firm located in San Jose, California, US is seeking a highly experienced Senior Clinical Research Scientist to contribute to groundbreaking scientific research and development. This hybrid role is crucial for designing, implementing, and overseeing clinical trials for novel therapeutic agents. The ideal candidate will possess a deep understanding of clinical trial methodologies, regulatory requirements (e.g., FDA, EMA), and data analysis. Responsibilities include developing clinical protocols, writing Investigator's Brochures, preparing regulatory submissions, and collaborating with Principal Investigators and site staff to ensure the successful execution of clinical studies. You will also be responsible for analyzing clinical data, interpreting results, and contributing to scientific publications and presentations. Strong project management skills and the ability to manage multiple research projects concurrently are essential. Experience with Phase I-IV clinical trials and knowledge of GCP (Good Clinical Practice) guidelines are mandatory. A Ph.D. or Master's degree in a life science discipline (e.g., Biology, Pharmacology, Biochemistry) is required, along with a minimum of 6 years of experience in clinical research. Excellent written and verbal communication skills, strong analytical abilities, and the capacity to work effectively in a team-oriented, cross-functional environment are critical. This role offers the flexibility of hybrid work, combining remote research and analysis with essential in-person collaboration at our state-of-the-art facility in San Jose, California, US .

Our client , a leading pharmaceutical innovator, is seeking a highly skilled and experienced Senior Clinical Research Scientist to join our esteemed R&D team in San Diego, California, US . This critical position will play a central role in the design, execution, and interpretation of clinical trials for novel therapeutic agents. The ideal candidate will possess a strong scientific background, extensive experience in clinical development, and a passion for advancing patient care through groundbreaking research.

As a Senior Clinical Research Scientist, you will be responsible for:

• Contributing to the development of clinical trial protocols, including study design, objectives, endpoints, and statistical considerations.
• Providing scientific and clinical input throughout the lifecycle of clinical studies, from concept to regulatory submission.
• Collaborating with cross-functional teams, including data management, biostatistics, regulatory affairs, and clinical operations, to ensure the successful implementation and monitoring of trials.
• Analyzing and interpreting clinical trial data, preparing study reports, and contributing to scientific publications and presentations.
• Ensuring all clinical research activities are conducted in compliance with Good Clinical Practice (GCP), regulatory guidelines, and internal SOPs.
• Identifying and evaluating potential new drug candidates and therapeutic areas for development.
• Engaging with external investigators, key opinion leaders (KOLs), and scientific advisory boards.
• Supporting the preparation of regulatory submission documents, such as Investigational New Drug (IND) applications and New Drug Applications (NDAs).
• Mentoring junior scientists and contributing to the scientific growth of the team.
• Staying current with scientific literature, emerging technologies, and regulatory advancements in the pharmaceutical industry.
• Participating in the evaluation and selection of CROs and other vendors.

Key qualifications required include:

• Ph.D. or M.D. degree in a relevant scientific discipline (e.g., Pharmacology, Biology, Medicine, Pharmacy).
• Minimum of 5-7 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
• Proven experience in clinical trial design, execution, and data analysis.
• Deep understanding of drug development processes and regulatory requirements (FDA, EMA).
• Excellent scientific writing and communication skills, with a track record of publications and presentations.
• Strong analytical and critical thinking abilities.
• Ability to work independently and collaboratively in a team environment.
• Proficiency in statistical analysis software and clinical data management systems is a plus.
• Demonstrated leadership potential and experience in managing complex projects.
• A strategic mindset and the ability to contribute to long-term research strategies.

This is an exceptional opportunity to make a significant contribution to the development of life-changing medicines. Join a highly collaborative and scientifically driven team.

Our client is seeking a highly experienced and motivated Senior Clinical Research Scientist to join their innovative pharmaceutical team in Phoenix, Arizona, US . This critical role involves leading and contributing to the design, execution, and analysis of clinical trials for novel drug development. The ideal candidate will possess extensive knowledge of pharmaceutical research, clinical trial methodologies, regulatory guidelines (FDA, EMA), and biostatistics. Responsibilities include developing clinical trial protocols, overseeing study conduct, managing data analysis, interpreting results, and contributing to regulatory submissions. You will work closely with cross-functional teams, including R&D, regulatory affairs, medical affairs, and clinical operations, to ensure the successful progression of clinical programs. The Senior Clinical Research Scientist will be responsible for literature reviews, scientific exchange, and potentially presenting study results at scientific meetings. A strong background in a relevant therapeutic area (e.g., oncology, immunology, cardiovascular) is highly desirable. Proficiency in statistical software and a deep understanding of data interpretation are essential. This position requires excellent scientific judgment, critical thinking skills, and the ability to manage multiple projects concurrently in a fast-paced environment. Excellent written and verbal communication skills are crucial for preparing study protocols, reports, and regulatory documents. This is an exceptional opportunity to contribute to life-saving therapies and advance your career in a leading pharmaceutical company that is committed to scientific excellence and innovation.

Key Responsibilities:

• Design and develop clinical trial protocols.
• Oversee the execution of clinical studies, ensuring compliance with protocols and regulations.
• Analyze and interpret clinical trial data.
• Prepare clinical study reports (CSRs) and contribute to regulatory submissions.
• Collaborate with cross-functional teams throughout the drug development process.
• Provide scientific and clinical expertise in a designated therapeutic area.
• Stay abreast of scientific literature and emerging trends in clinical research.
• Evaluate and implement new technologies and methodologies in clinical trials.
• Participate in scientific meetings and discussions.
• Mentor junior research staff.

Qualifications:

• Ph.D. or Pharm.D. in a relevant scientific or medical field.
• Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
• In-depth knowledge of clinical trial design, conduct, and data analysis.
• Familiarity with ICH-GCP guidelines and regulatory requirements.
• Experience in a specific therapeutic area is highly preferred.
• Proficiency in statistical analysis and interpretation of clinical data.
• Excellent scientific writing and communication skills.
• Strong analytical and problem-solving abilities.
• Ability to manage complex projects and work effectively in a team.
• Proven ability to contribute to regulatory submissions (e.g., IND, NDA).