The company is seeking a dedicated MD or DO to join their team as a Principal Investigator for clinical trials in women's health. This role is ideal for a full-time physician looking to diversify their income and provide additional support to their patients through clinical research. The position offers a flexible time commitment, competitive compensation, and the opportunity to enhance patient care through participation in cutting-edge clinical research.

Principal Investigator (MD/DO) for Clinical Trials

Principal Investigator for Clinical Trials

Westat is seeking a highly motivated and experienced Associate Vice President with strong business development, client management, project leadership, and clinical research experience to join the leadership team in the Clinical Research Practice. This role involves spearheading business development in clinical research, managing large-scale projects, and securing contracts with federal agencies, specifically targeting the Department of Health and Human Services. The position is remote and focuses on growing the company's clinical research services within HHS agencies.

ASSOCIATE VICE PRESIDENT, CLINICAL RESEARCH (CLINICAL TRIALS) REMOTE

Associate Vice President, Clinical Research

The Clinical Research Associate at Ascendion is responsible for managing clinical activities at study sites, fostering strong relationships within the organization, and overseeing the performance of appointed study sites. This role involves conducting site visits, monitoring, communication, and delivering on assigned study sites, serving as a liaison between Clinical Operations and study site personnel.

Clinical Research Associate

The Clinical Trial Associate (CTA) will work with the Clinical Operations team to support the conduct of clinical trials. This role involves supporting various clinical trials and managing certain aspects of the clinical trials, partnering with Clinical Project Managers and Clinical Trial Managers to ensure studies are completed on time, within budget, and in compliance with SOPs, FDA regulations, and ICH/GCP guidelines. This is a fully remote, contract position with a duration of 6 months.

Clinical Trial Associate 100% Remote

Clinical Trial Associate

The Principal Biostatistician is responsible for providing statistical support for drug development programs in early phases of development, focusing on healthy normal studies with PK and PD endpoints. This role involves collaborating with multidisciplinary project teams, establishing project timelines, providing statistical input to study protocols, and contributing to regulatory documents such as clinical study reports and DSURs. The position offers home-based remote working opportunities, a flexible schedule, and a focus on bringing new therapies to market.

FSP PRINCIPAL BIOSTATISTICIAN FOR EARLY PHASE CLINICAL (PK)

Principal Biostatistician for Early Phase Clinical (PK)

As a Principal Business Consultant in R&D Clinical at Veeva Systems, you will be part of a unique group fusing strategy and operations with data and technology to transform the life sciences industry. This role involves leading business development opportunities, leveraging networks to identify opportunities, building strong customer relationships, and supporting multiple project engagement teams. The position requires significant management and R&D consulting experience, particularly in the clinical operations area of Life Sciences, and offers the opportunity to work remotely.

PRINCIPAL BUSINESS CONSULTANT - R&D CLINICAL

Principal Business Consultant - R&D Clinical

The Clinical Scientist at Hydrogen Group will contribute to the design, implementation, review, and communication of clinical protocols and study reports for scientific and operational accuracy. This role involves analyzing data, delivering high-quality clinical study data analysis for publications and scientific presentations, and collaborating with the Medical Director and Clinical Operations to expedite the execution of clinical trials. The position requires a strong background in oncology clinical trials and a minimum of 8-10 years of industry experience.

Remote Clinical Scientist (Must have strong Oncology exp)

Clinical Scientist

The Scientist 3 - Clinical Research at US Tech Solutions is responsible for the translation and implementation of scientific concepts into study design and/or program across planning, execution, and reporting. This includes integrating biomarkers, digital technologies, data science initiatives, and select vendors. The role is remote but requires residing in the Eastern Time Zone and involves being onsite once every two weeks in Titusville. The position requires at least a Bachelor's degree in a Life Science category, Pharma and/or Clinical experience, and specific expertise in Neurosciences, data review, and clinical development.

Scientist 3 - Clinical Research

The Care Researcher at Care.com is responsible for researching, finding, and contacting resources that support and assist clients. This role involves locating community-based resources to match clients' needs, which may include alternative housing, financial assistance, mental health resources, home repairs, relocation, pet sitting, and health & wellness. The position is remote but requires a dedicated 8-hour work day.

Researcher

The Clinical Scientist at Actalent will collaborate with clinical teams for a specific product candidate, designing, preparing, and initiating study protocols and other required documentation in compliance with project plans, federal regulations, GCP, and good medical practice. This role involves conducting literature research, working with the medical monitor to assist clinical sites in the efficient completion of clinical trials, and collaborating on the development of study-related materials. The position requires strong analytical skills, business communication skills, and the ability to deliver high-quality scientific presentations.

Stanford University is seeking an Assistant Clinical Research Coordinator to perform administrative support duties related to the collection of clinical data and/or the coordination of clinical studies. This role involves working under the supervision of the principal investigator and/or study coordinator/supervisor, and is part of the Childhood Research Obesity Prevention Lab within the Department of Pediatrics, Division of Gastroenterology, Hepatology, and Nutrition. The position supports the Pediatric GI Division's mission of healing children with digestive disease through innovation, and requires a two-year college degree and relevant experience or an equivalent combination of experience, education, and training.

Assistant Clinical Research Coordinator

The Clinical Research Associate at Kelly Services will be responsible for ensuring clinical trials are completed on-time, according to the protocol, and for keeping clients and sites informed throughout the process. This role involves managing diagnostic clinical studies, developing and managing protocols, case report forms, budgets, and regulatory documents, as well as monitoring clinical studies and managing site relationships. The position is remote, permanent, and offers the opportunity for career growth within a growing clinical research company.

PeaceHealth is seeking a RN Clinical Research for a Per Diem/Relief, 0.00 FTE, Day position. The role involves participating, conducting, and managing clinical research studies, acting as a liaison between the clinic and the outside sponsoring firm, and coordinating and managing patient participation and data management for assigned studies. The position requires an Associate Degree in Nursing, a minimum of 3 years of nursing experience, and offers a salary range of $46.46 - $69.68.

RN Clinical Research- Remote

RN Clinical Research

The Manager of Clinical Trial Strategy and Submissions at AbbVie is responsible for delivering regulatory strategies and operations for a designated portfolio of development compounds globally. This role involves ensuring compliance with global regulatory strategies, managing study deliverables, interfacing with regulators and global subject matter expert functions, and maintaining regulatory databases. The position can be based remotely within the US.

Manager, Clinical Trial Strategy and Submissions (Remote)

Manager, Clinical Trial Strategy and Submissions

The Lead Research Scientist at the Institute for Health Metrics and Evaluation (IHME) will drive analytic innovation, supervise and mentor junior staff, and participate in leadership responsibilities for the Future Health Scenarios team. This role involves managing research team staff, developing custom scenarios for future health outcomes, and presenting results to various audiences. The position requires a strong command of forecasting models, the ability to supervise and mentor junior staff, and a commitment to improving health outcomes globally.

Lead Research Scientist, Future Health Scenarios

Lead Research Scientist

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