Clinical Study Manager
$40 - $80 per hourAlignerr
Clinical Study Manager
$40-80/hr Remote Freelance STEM
About the Role
What if your clinical trial management expertise could directly shape how AI understands and reasons about one of the most complex, high-stakes fields in the world? We're looking for experienced Clinical Study Managers to help build and validate AI systems trained on real-world clinical research data — bringing rigor, precision, and operational know-how to the frontier of AI development.
This is a fully remote, flexible contract role. You'll apply your deep knowledge of clinical trial operations to evaluate, annotate, and improve AI outputs — helping ensure these models reflect the standards and realities of professional clinical research.
What You'll Do
- Oversee and evaluate AI-generated content related to clinical trial operations, timelines, budgets, and vendor management
- Apply your real-world clinical research expertise to assess the accuracy, completeness, and quality of AI outputs
- Manage and review simulated or real clinical trial workflows, milestones, and deliverables as part of AI training datasets
- Identify gaps, errors, and inconsistencies in AI-generated clinical research content and provide structured, detailed feedback
- Coordinate across multiple workstreams to ensure study-related AI tasks are completed on time and to a high standard
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Experienced clinical trial professional with a strong background in study operations and project management
- Skilled at managing budgets, timelines, and vendor or CRO relationships across complex, multi-site studies
- Naturally detail-oriented with a systematic approach to identifying risks and resolving operational issues
- Clear and confident written communicator who can document findings precisely
- Self-motivated and reliable when working independently without close supervision
Nice to Have
- Prior experience with data annotation, data quality review, or AI evaluation workflows
- Familiarity with eClinical systems, EDC platforms, or clinical data management tools
- Background in regulatory affairs, GCP compliance, or clinical operations leadership
- Experience working across therapeutic areas or international multi-site trials
Why Join Us
- Work on cutting-edge AI projects alongside leading AI research labs and healthcare innovators
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, high-impact work
- Gain exposure to advanced large language models (LLMs) and how they're trained using real-world clinical expertise
- Contribute to AI development that has a genuine impact on the future of healthcare and clinical research
- Potential for ongoing work and contract extension as new projects launch
- ...Clinical Outsourcing & Vendor Management Lead outsourcing activities for clinical studies and other clinical development projects. Develop and execute sourcing strategies that align with program objectives, timelines, quality expectations, and budget requirements...SuggestedFull timeContract work
- ...executing them on time and within budget• Overall coordination and management of clinical trials from startup to closeout• Liaise with other... ...members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed...SuggestedWork at officeImmediate start
$93.1k - $232.8k
...bring breakthrough treatments to patients faster.Drive global clinical trials from first site activation to final patient visit—own... ...clinical research worldwide.Required Experience2+ years of global study management experience Experience across multiple countries/regionsPhase...SuggestedFull timeContract workPart timeWork at officeImmediate startWorldwide$140k - $180k
...technology, come be a part of our great team! POSITION SUMMARYThis position is for overseeing clinical activities related to one or more clinical studies and performing/managing the daily in-house operations associated with the studies. The Clinical Study Manager must be...SuggestedWork experience placementInterim roleLocal areaFlexible hours- ...Responsible for operational aspects of one or more clinical trials (phase I-IV, Expanded Access,... ...external focus• Contributes to or manage simple clinical trial with minimal supervision... ...Novartis Trials - provide feedback on study proposals, review submitted study concepts...SuggestedContract workWork at officeLocal areaImmediate start
- ...labor as a variable cost.Job DescriptionJob Description: • The Non-MD/Study Clinician integrates scientific drug development knowledge to ensure excellence in development and translation of clinical research plans into efficiently delivered studies.• The Non-MD/Study Clinician...Immediate start
- ...cost.Job Description1. Support individual clinical trial teams (CTTs) and Biomarker Sub-... ...liaising with internal stakeholders. Assist Study Lead by forecasting the biosample... ...analysis, and assisting with the relevant data management components. 4. With support, provide...Work at officeImmediate start
$102k - $162k
Job TitleClinical Study ManagerJob DescriptionClinical Study Manager, Sleep & Respiratory CareThe Clinical Study Manager oversees the execution and regulatory compliance of clinical studies, managing documentation, negotiations, and team priorities to ensure program objectives...Full timeWork at officeLocal areaImmediate startWork visaRelocation package3 days per week$54.48 per hour
...Clinical Trial Program Manager W2 Contract 12-Months, Possible Extension $54.48hr + Benefits San Diego, CA, 92103 Summary We are seeking... ...professional to support clinical operations activities, study deliverables, documentation, data review, and cross-functional...Contract work- ...opportunities Job Description We are seeking a strategic Clinical Marketing Manager to drive downstream marketing, product adoption, and... ...Campaign Development: Transform complex clinical data and case studies into clear, impactful marketing collateral and promotional...Full timeTemporary workLocal area
$115k
## Clinical Study ManagerApply: Remote - USA: Full time: Posted 2 Days Ago: R5483NAMSA pioneered the industry and was the first independent... ...Target:** $115,000.00**Job Description:**Clinical Study Managers (CSM) are responsible for the timely execution and high quality...Full timeContract workLocal areaRemote work- ...physician, a health coach navigator, and a physical therapist who manage the initial patient assessment and then work to coordinate all... .... Reporting to the Director of Central Operations, the Clinical Practice Manager oversees the administrative operations supporting...Work at officeImmediate startRemote workWork from homeFlexible hours
$113.3k - $226.7k
...than 160 countries.JOB DESCRIPTION:Sr. Clinical Publication ManagerWorking at AbbottAt Abbott... ...’ll Work OnThe Sr. Clinical Publication Manager in Electrophysiology designs and... ...for post-market clinical follow-up (PMCF) studies and registry data.Strategic Publication...Local areaWorldwideShift work$164k - $205k
...patients.The Opportunity:This is a unique opportunity for a Clinical Operations Professional. As a Sr. Clinical Program Manager, you will be responsible for acting as a central contact for the Clinical Study Team(s) and assist with the execution and management of Revolution...Full timeContract workTemporary workWork at officeLocal areaWorldwide- ...Responsible for performing the ongoing review of clinical trial data as outlined in the data... ...trila duration in collaboration with management.Collaborate with Medical Lead/BSL to identify... ...and publishing global clinical studies in a pharmaceutical company or contract...Contract workWork experience placementWork at officeImmediate start
$116k - $182.27k
...DescriptionAre you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as a Lead Clinical Study Manager based remotely reporting to the Clinical Operations Leadership team.At Takeda, we are transforming the pharmaceutical...Minimum wageContract workInterim roleLocal areaRemote workNight shift- ...Gilead and help create possible, together.Job DescriptionThe Clinical Program Manager is responsible for the worldwide execution of all Phase I -... ...oversee and be responsible for the successful execution of studies and/or multiple studies within a program or multiple...Full timeContract workFor contractorsLocal areaWorldwide
- ...here.Job DescriptionPrimary Function of Position:The Senior Clinical Program Manager serves as the strategic and operational partner to Clinical... ...the Clinical Development & Operations portfolio from study startup through regulatory submission. The role partners with...Contract workLocal areaWorldwideFlexible hours
- Job SummaryOur clinical operations activities are growing rapidly, and we are currently seeking a full-time, Clinical Safety Manager to join our Clinical Safety Department. This position plays... ...;Provide safety review of clinical study documents, including protocols,...Full timeContract workWork from home
- ...DescriptionLeads the cross-functional execution of one or more clinical studies conducted within the Pharmaceutical Clinical Research Unit (... ...development efforts, verification of EDCMS study set up, management of cross-study activities and coordination of PCRU functional...Local areaImmediate start
- ...ApplicationsEmail: ****@*****.*** Opportunity: Clinical Program Manager (CPM)This is a unique opportunity for a Clinical Program... ...and begins to develop new ideas.Lead the Clinical Study Execution Team (CSET) meetings and ensure trial timelines are...
$143k - $178k
...patients.The Opportunity: This is a unique opportunity for a Clinical Operations Professional. As a Clinical Program Manager (CPM), you will be responsible for acting as a central contact for the Clinical Study Team(s) and assist with the execution and management of...Full timeContract workWork at officeLocal areaWorldwide$117k - $145k
...About Kalaris Kalaris Therapeutics is a clinical stage biopharmaceutical company... ...diseases. In head-to-head preclinical studies, TH103 showed more anti-VEGF activity and... ...development. Kalaris’ board of directors, management team and investors include co-founders,...Interim roleWork at officeNight shift- ...planning, direction and implementation of clinical systems for data collection which may... ...planning, vendor oversight, EDC build and study timelines, etc. Perform or provide... ...create Data Validation Specifications, Data Management Plans, eCRF Completion Guidelines, and Data...
- Job-ID31716268Reference26-00054 Responsibilities: Maintain and update EDC user access across multiple clinical studies Track and manage user access requests in coordination with CRAs and EDC vendors Curate and maintain standardized tracking spreadsheets for both internal...
$170k - $190k
The Senior Clinical Trial Drug Supply Manager is a critical position within the clinical development organization directly supporting the execution... ...submissions. This role will be responsible for multiple global studies and the independent oversight of drug supply forecasting...Temporary workWork at officeFlexible hours- Job-ID31629249Reference25-04683 Responsibilities: Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. Develop and manage data management timelines for multiple projects, ensuring all milestones...
- ...Reference24-01196 Responsibilities: Collaborate with data managers, statistical programmers, biostatistics, clinical operations, and external vendors to review, sign... ..., dashboards, and reconciliation reports for all studies. Participate in developing and implementing SAS...Work experience placement
- ...about Artivion, visit our website, . Position Overview: The Sr. Clinical Data Manager is responsible for data management operations and for the... ...and execution of data management activities for assigned studies and projects. This includes but is not limited to database set...Full timeWorldwide
- ...ID31811474Reference26-00190 Responsibilities: Represent Data Management in study team meetings, providing metrics and guidance on data-... ...project documentation in an audit-ready manner. Support Lead Clinical Programmers in developing and managing Data Transfer Agreements...
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