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Results for "Clinical Trials"

11 gigs found around $100 across all platforms

AllDesign & CreativeDesign & Creative83Development & TechDevelopment & Tech518Writing & ContentWriting & Content22Marketing & SEOMarketing & SEO118Business & ConsultingBusiness & Consulting250Video & AnimationVideo & Animation5Music & AudioMusic & Audio4
HimalayasView price

Senior Azure Data Engineer

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Job Purpose : To ensure smooth promotion, operation, and reliability of data and technology pipelines across environments. This role is responsible for maintaining strong alerting and monitoring systems and ensuring all workflows run consistently with no disruptions or surprises. Key Accountabilities : Monitor and manage Databricks workspaces across Dev, QA, and Prod environments. Troubleshoot job failures, cluster performance issues, and workspace

Data EngineeringAzure Data EngineeringCloud Engineering
India
about 8 hours ago
HimalayasView price

CRA I/II - FSP - Belgium **Attractive Sign On Bonus for starters by end of 2025*

Work Schedule Other Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Location/Division Specific Information PPD's Functional Service Provider division partner with and serve as an extension of our

Clinical Research AssociateCRAClinical Operations
Belgium
HimalayasView price

Senior Clinical Research Associate (Brazil)

We’re expanding our capabilities across Latin America , and we’re hiring a Senior Clinical Research Associate to support critical studies across Brazil! As a Senior CRA you'll posses a wide-ranging and broad experience handling our most complex and advanced assignments. Responsibilities will be dependent upon the type and timing of the program to which the Senior CRA is assigned and will, at a minimum, include start-up and study implementation activities, on-site monitoring of clinical research studies as well as on-going site management. Incumbents are expected to be able to manage appropriately sized or complex clinical trials, and support Clinical Trial Managers and/or Project Managers with trials as required. An increased focus on training and mentoring junior staff members may be expected. Responsibilities: Independently oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low que

Clinical Research AssociateClinical ResearchClinical Monitoring
Brazil
HimalayasView price

Local Clinical Trial Manager - FSP, Israel

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for

Clinical Trial ManagementClinical Research AssociateClinical Operations
Israel
HimalayasView price

Sr Medical Manager PSS

Summary of Responsibilities: Responsible for medical review of serious adverse events and adverse events of special interest from clinical trials in support of drug safety activities for clients. When applicable, responsible for preparation and medical review of Aggregate Reports required by global regulatory agencies for review of safety information for assigned products, when authorized to perform this function on behalf of a client. When applicable, responsible for signal detection and evaluation activities and preparation and submission of Ad Hoc Reports reviewing specific safety issues to the global regulatory agencies for assigned products, when authorized to perform this function on behalf of a client. Participates in training opportunities to advance knowledge of pharmacovigilance as it relates to drug/product development and drug/product marketing utilizing good clinical practice guidelines. Provides medical/safety expertise to project teams, including communicating informati

PharmacovigilanceDrug SafetyMedical Affairs
India
HimalayasView price

Associate Software Engineer

Join Clario and help transform lives by unlocking better evidence. In this role, you’ll design and develop software applications that support clinical trials and life-changing therapies. If you’re passionate about technology and want to make an impact in healthcare, we’d love to hear from you. What We Offer Competitive compensation and incentive plans Provident Fund and comprehensive medical insurance Employee wellness programs and engagement activities Flexible work arrangements and modern office facilities What You’ll Be Doing Provide technical design for software applications Create or update software documentation to reflect current architecture Participate in code reviews as needed Update existing applications based on user story changes and enhancements Perform unit testing, validation, and documentation for new and updated applications using appropriate protocols and techniques Offer technical support and guidance to internal and external users by: Answering questions on applic

Software EngineeringSoftware DevelopmentAssociate Software Engineer
India
HimalayasView price

Vendor Alliance Lead Associate Director

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities: Operational Management / Deliverables Works within a matrix environment, the VCE is accountable for all operational aspects of 1 or more ERMTs May oversee a team of Vendor Startup Managers (VSM) or Imaging Operation Managers (IOM) including assignment of trial level support, and as a point of escalation in addition to oversight responsibilities. Supplier Service or Equipment expert for the assigned services within the ERMTs to

Vendor ManagementClinical OperationsStrategic Sourcing
India
HimalayasView price

Global Study Manager II - FSP

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel FSP is looking for Global Study Managers in Argentina, Brazil or Mexico! Job Summary The Global Study Manager II (GSM II) provides operational leadership throughout the study lifecycle, with accountability for oversight and execution of study management, site management, preferred Contract Research Organization (pCRO), and vendor deliverables for all study management deliverables in a study. The Global Study Manager has exceptional knowledg

Clinical ResearchClinical Trial ManagementStudy Management
Mexico
HimalayasView price

Senior Director, Project Mgt - Ophthalmology Trials Team - Remote based in the U

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Position requires Sr Director - (Oversight function) level person with a demonstrated expertise managing global Ophthalmology clinical trial portfolios. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communiti

Project ManagementClinical ResearchClinical Operations
United States
HimalayasView price

Business Development Manager

About Profound Research Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies while maintaining the trusted patient-physician relationship. Our Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues. Solution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency. Excellence: W

SalesBusiness DevelopmentClinical Research Business Development
United States
HimalayasView price

Clinical Trial Manager - FSP

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities : Manage external vendors and contract research organizations Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents Assist with protocol development and study report completion Manage monitoring activities (may

Clinical ResearchClinical OperationsClinical Trial Management
United Kingdom
about 19 hours ago
5 days ago
7 days ago
7 days ago
8 days ago
8 days ago
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8 days ago
13 days ago
14 days ago