Clinical trials jobs

Consultant, Clinical Supplies Management, Biopharma, Global Trials

Remote or Almont, Colorado

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Today

Description: CONTEXT & INITIATIVE DESCRIPTION Our BioPharma Client is seeking a Consultant, Clinical Supplies Management to support the planning and execution of global Phase I- clinical trials. This critical Consultant will play a key role in ensuring the timely availability, packaging, distribution, and ongoing management of clinical trial supplies across sites and depots. The ideal candidate will have strong clinical supply and trial operations experience, excellent cross-functional communi

Contract

Clinical Research Scientist III - (Director/Assoc. Director level)

Remote or Hybrid in Parsippany-Troy Hills, New Jersey

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30+d ago

Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols. Participates in protocol review discussions concerning scientific and procedural aspects of study design. Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks, and other documents as needed with appropriate guidance and supervision. With supervision, contributes to the design and development of CRFs, Data Management Manuals and Da

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Contract, Third Party

$100 - $110

Director/Senior Director - CRO Solutions & Product Strategy

Remote

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18d ago

Director/Senior Director - CRO Solutions & Product Strategy Company: Saama Function: Product / Solutions Level: Director or Senior Director Location: RemoteSaama is an AI and advanced analytics company built for life sciences. Best known for the AI-powered clinical platform that supported the trial behind the worlds first COVID-19 vaccine, Saama works with many of the top 20 pharmaceutical companies and a large base of emerging biotechs. Alongside our clinical development portfolio, we operate a

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Full-time, Third Party

Depends on Experience

Clinical Research Associate I - Pulmonary Research Program/Lung Institute

Beverly Hills, California

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Today

Job Description Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements! Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world. The Pulmonary Research team at the Cedars?Sinai Women\'s Guild Lung Institute comprises a group of world-class researchers whose combined interests span multiple fields. The unified go

Full-time

Clinical Operations Analyst - Remote / Telecommute

Sacramento, California

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Today

We are looking for Clinical Operations Analyst - Remote / Telecommute for our client in Sacramento, CAJob Title: Clinical Operations Analyst - Remote / Telecommute Job Location: Sacramento, CA Job Type: Contract Job Overview: Pay Range: $39.31hr - $44.31hr Requirement/Must Have: Bachelor s Degree or Equivalent in Computer Science, Engineering, Business or related field.2-4 years of patient screening experience in the setting of a clinical trial.Good computer skills in Microsoft Office Suite, inc

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Third Party, Contract

Depends on Experience

Lab Technician

San Diego, California

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25d ago

Job: Lab Technician, Neuroscience Biomarkers Immunoassays Duration: 08/31/2026 to 12/31/2026 with possible extension Location: San Diego, CA 92121 (Onsite) Description: The Lab Technician, Biomarkers Protein Lab is a member of the Neuroscience Precision Biomarkers team, and is responsible for creating and validating assays, executing them, planning experiments, and implementing immunoassays on clinical samples. They maintain equipment and ensure laboratory safety by identifying problems and co

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Contract

$33 - $38

Clinical Research Associate I - Heart Institute - Berman Lab

Beverly Hills, California

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Today

Job Description Grow your career at Cedars-Sinai! . When you join our team, you?ll have access to groundbreaking biomedical research facilities and world-class medical education programs. We take pride in hiring exceptional, dedicated professionals who are passionate about advancing healthcare. Our physicians, nurses, and staff reflect the culturally and ethnically diverse communities we serve and are united by a shared commitment to excellence. Together, we foster a dynamic, inclusive environme

Full-time

Clinical Safety Monitor

Maple Grove, Minnesota

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10d ago

Clinical Safety Monitor Location: Maple Grove, MN (Onsite) Experience: 5+ years Role Summary The Safety Monitor ensures that clinical studies are planned and conducted in compliance with applicable regulations, Good Clinical Practices, and standard operating procedures. The primary focus of this role is the processing and review of adverse events, ensuring the consistency, completeness, and regulatory compliance of safety data for assigned studies. Key Responsibilities Processes all adverse eve

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Full-time, Third Party

Depends on Experience

Clinical Study Administrator

Remote or Irvine, California

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Today

Kelly Science and Clinical FSP is currently seeking a Clinical Study Administrator for a long-term engagement with one of our Global MedTech clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be e

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Contract

Clinical Trial Manager

Remote or Almont, Colorado

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Today

Description: Remote Our client is seeking a Clinical Trial Manager to oversee 2-3 Phase global clinical studies in the MASH therapeutic area across Europe. The role provides sponsor-side oversight of fully outsourced studies executed by a CRO partner, reporting to the Clinical Operations Program Lead. The Clinical Trial Manager will lead study governance, manage timelines and risks, ensure quality and compliance, and coordinate cross-functional teams to drive successful study execution. Due

Contract

Clinical Research Associate (Portuguese Fluency)

Boston, Massachusetts

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Today

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Research Associate (Portuguese Fluency) for a Contract assignment with one of our premier Healthcare clients in Boston, MA. * 70% will be traveling to and from sites and 30% will be completed remote at home* Responsibilities : Ability to prioritize workload and manage multiple protocols Contribute to the identification of new sites for clinical trials Implement complete site management including monitoring visits and regu

Contract

USD 65.00 - 80.00 per hour

Lead Clinical Research Coordinator (Full Time, Days)

Miami, Florida

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Today

DescriptionJob Summary Under direction of a Research Clinical Trial Operations leader, the Lead Clinical Research Coordinator CTO will independently coordinate and will be accountable for the overall administration and outcome of multiple clinical studies within the Clinical Trials Office, requiring advanced-level knowledge and skills, involving human subjects that are being conducted within the Nicklaus Children\'s Research Institute. Ensures processes are in place and roles are defined in ord

Full-time

Heart Institute - Clinical Research Associate I, Susan Cheng Team

Los Angeles, California

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Today

Job Description The Smidt Heart Institute reflects Cedars-Sinai\'s steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From

Full-time

Clinical SAS Programmer

King of Prussia, Pennsylvania

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30+d ago

Design, develop, and validate statistical programs, datasets, and reporting outputs (tables, listings, and figures) for clinical trials in alignment with project requirements and regulatory standards. Build and maintain analysis datasets (ADaM) and study data tabulation models (SDTM) in compliance with CDISC standards, ensuring traceability and submission readiness. Develop, maintain, and optimize SAS programs, macros, and templates for clinical data review, reconciliation, and reporting to supp

Full-time

Field Clinical Research Associate

Washington, District of Columbia

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6d ago

Field Clinical Research Associate USA - Los Angeles, CA, Tampa or Orlando, FL, and Washington, DC/ Philadelphia, PA Role SummaryThe Field Clinical Research Associate (Field CRA) is responsible for monitoring clinical research sites to ensure compliance with study protocols, ICH-Google Cloud Platform requirements, applicable regulatory requirements, and sponsor procedures. The Field CRA serves as the primary monitoring resource for assigned sites, conducting routine site visits, reviewing study d

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Full-time

Depends on Experience

UKG Workforce Mgmt Systems Analyst II SR

Menomonee Falls, Wisconsin

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7d ago

Discover. Achieve. Succeed. #BeHere Location: US:WI:MENOMONEE FALLS at our WOODLAND PRIME 400 facility. This job is REMOTE. FTE: 1.000000 Standard Hours: 40.00 Shift: Shift 1 Job Summary: This position uses defined methodologies in a team environment to perform system life cycle tasks for assigned systems or applications and supporting infrastructure. These tasks include planning, system analysis, design, application building, integration, testing, maintenance, support and the completion o

Full-time

USD 34.82 - 59.56 per hour

Principal Medical Writer

King of Prussia, Pennsylvania

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Today

Job Description\n \n The Principal Medical Writer is a key leadership position responsible for determining and driving the medical writing strategy for one or more Programs within Clinical Development. \n \n \n The incumbent is accountable for the efficient preparation of high quality, strategically aligned medical writing deliverables that support the clinical development, clinical safety and regulatory requirements of a clinical program. He or she is also responsible for the messaging strat

Full-time

Sr. Clinical Trial Manager (CTM), Late Phase EU Metabolic Studies - Region Lead

Remote or Almont, Colorado

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Today

Description: Remote Our client seeks a Senior Clinical Trial Manager to lead sponsor-side oversight for Phase global studies across Europe in the MASH therapeutic area. The role will provide regional leadership of fully outsourced studies, manage EU submissions, oversee site activation, and guide two sponsor-side CTMs assigned to specific countries. The CTM will drive governance with the CRO, ensure quality and compliance, and collaborate with cross-functional teams to meet timelines. The pos

Contract

Clinical Trial Manager

Remote or Almont, Colorado

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Today

Description: Remote Our client seeks three Clinical Trial Managers to join an established Clinical Operations FSP program. The CTM will oversee assigned clinical trials with a focus on vendor and CRO management, study execution, and financial and milestone tracking. The role ensures compliance with ICH Google Cloud Platform, regulations, protocols, and SOPs while collaborating with internal teams, clinical sites, and external partners. The CTM reports to Clinical Operations leadership and may

Full-time

USD 115,000.00 - 120,000.00 per year

Director, Portfolio Development Process & Standards Lead

King of Prussia, Pennsylvania

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Today

Job DescriptionCSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. \n \nCould you be our next Director, Portfolio Development Process & Standards Lead? This position is located in our King of Pru

Full-time

Compensation information provided in the description