Entry Level Clinical Analyst Jobs

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Project Manager - Clinical R&D (Pharma)

HR Link Group, Inc

•

Remote

Third Party, Contract

ROLE: Project Manager - Clinical R&DDURATION: 8+ mo / REMOTEVISA: h1b okDomain: PharmaceuticalsRate: your best rate . ** CLINICAL R&D Experience is a MUST AI experience is a plus ! Clinical R&D Background: Experience of working in a Clinical R&D organization or a division of a large pharma company. clinical trials, including patient recruitment, trial design, data management, monitoring, R&D Pipeline management, regulatory submission etc (at least a few of them)Support implementation of syste
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Posted 3 days ago | Updated 1 day ago

Clinical Research Associate

GForce Life Sciences

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Sunnyvale, California, USA

Full-time

Job DescriptionSr. Clinical Research Associate 12-month contract Onsite in Sunnyvale, CA Responsibilities Support the successful execution of clinical studies by contributing to study design, documentation, and overall management.Lead and manage site start-up and activation processes, including regulatory document preparation, IRB/EC submissions, and clinical trial agreements.Conduct monitoring visits (qualification, initiation, interim, and close-out) and ensure protocol and regulatory complia
Posted 8 days ago | Updated 1 hour ago

Statistical Programmer (Clinical Trials)

Ledgent Technology

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Remote

Contract

We are seeking a Statistical Programmer to work on a remote team for a project with our client. The preferred R stack experience includes dplyr, rmarkdown, dbplyr, ggplot2, roxygen, and plotly to solve complex challenge. We are unable to work with 3rd party candidates. Summary The main function of Sr. Analyst is to develop, validate datasets, tables/listing/figures using SAS/R programming language, and other ad-hoc request to support business requirements. Job Responsibilities *In this rol
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Posted 9 days ago | Updated 3 hours ago

Clinical Research Associate

GForce Life Sciences

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Alameda, California, USA

Full-time

Job DescriptionClinical Research Associate 6-month contract - highly likely to extend Onsite in Alameda 5 days per week Key Responsibilities: Proactively identify and address issues related to study monitoring and site management.Track and communicate monitoring updates and site performance; escalate risks to clinical leadership as needed.Support internal processes such as onboarding, protocol training, and maintenance of monitoring tools and study documentation templates.Manage and oversee CR
Posted 18 days ago | Updated 13 hours ago

Clinical QA Lead

Bahwan CyberTek Inc.

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Boston, Massachusetts, USA

Third Party, Contract

Title : Clinical QA Lead Location: Boston, MA (Hybrid) Duration : Long term Description: Minimum of 8 years of software quality testing experience and 12+ years IT/Industry experience. 5+ years of experience in Computer Systems Validation (CSV) in the context of Good Clinical/Manufacturing Practices (GxP) is preferred. Experience with software application test planning and functional testing, performance testing, developer management, and defect management using Application lifecycle management
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Posted 25 days ago

Clinical SME with AI/GenAI Experience New York for contract

BURGEON IT SERVICES LLC

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New York, New York, USA

Contract, Third Party

Job Title: Clinical SME with AI/GenAI Experience Location: Hybrid (Onsite as needed) Client Location: New York Contract Duration: 6 Months (Starting July) pranayatburgeonitsdotcom Experience Required: Total Experience: 10+ yearsRelevant Experience: 10+ years in Clinical R&D, GenAI, and Project ManagementMandatory Skills: Expertise in Clinical R&DExperience with Generative AI tools and applicationsStrong Project Management capabilitiesEffective in matrix environments with clinical, regulatory, a
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Posted 4 days ago

Clinical Trial Manager

Scientific Search

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Morristown, New Jersey, USA

Full-time

Job DescriptionLocation: Morristown, NJ/Hybrid Base Salary up to $150k plus bonus and LTI. Our biopharmaceutical client located in Northern NJ area has tasked Scientific Search with finding a Clinical Trial Manager. This role is responsible for supporting study management activities for clinical studies in compliance with Standard Operating Procedures (SOPs), ICH-GCP, clinical study protocol and all applicable regulatory requirements. Responsibilities Ensures that study conduct is in accordan
Posted 18 days ago | Updated 1 hour ago

Clinical Research Coordinator

Zachary Piper Solutions, LLC

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Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a highly organized and proactive Clinical Research Coordinator (CRC) to support clinical trials across multiple therapeutic areas on-site in the Raleigh, NC area. This role is essential in ensuring smooth trial execution within a clinical site network, with a focus on phlebotomy and patient coordination. Key Responsibilities of the Clinical Research Coordinator: Oversee day-to-day clinical trial activities while ensuring compliance with Google Cloud Platform, IRB, and
Posted 22 days ago | Updated 19 days ago

Manager-Vendor Performance Management(Clinical)

NexInfo Solutions, Inc.

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Morris Plains, New Jersey, USA

Contract, Third Party

About Nexinfo: NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challenges
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Posted 19 days ago | Updated 18 days ago

Clinical Data Manager

Tandym Tech

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Woburn, Massachusetts, USA

Contract

A pharmaceutical company in Massachusetts is currently seeking a new Clinical Data Manager to provide Data Management support for assigned programs. Responsibilities: Work with Clinical Data Management (CDM) Lead to support operational activities for one or more programs Monitor data management vendor quality of work through key performance metrics Maintain program level DM deliverable timelines in accordance with program development strategy Support data management at cross-functional team mee
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Posted 20 days ago | Updated 3 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Athens, Georgia, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 2 days ago | Updated 3 hours ago

Clinical Trial Manager

Advanced Recruiting Partners

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Raleigh, North Carolina, USA

Full-time

Job DescriptionKey Responsibilities: Lead and manage all operational aspects of global clinical trials from study start-up through close-outOversee study timelines, deliverables, and budgets to ensure milestones are metCoordinate with cross-functional teams, external vendors, and CROs to ensure high-quality study conductOversee site activation, clinical monitoring, data integrity, and adherence to protocolConduct study-level risk assessments and ensure inspection readinessManage safety and pharm
Posted 8 days ago | Updated 2 hours ago

Clinical Research Coordinator

Zachary Piper Solutions, LLC

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Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a detail-oriented and proactive Clinical Research Coordinator (CRC) to join our growing clinical research team. The ideal candidate will have hands-on phlebotomy experience and a strong background working within a clinical site network environment. This role is essential in supporting the execution of clinical trials across multiple therapeutic areas. Responsibilities for the Clinical Research Coordinator: Coordinate and manage day-to-day clinical trial activities in
Posted 30 days ago | Updated 19 days ago

Remote Clinical Ancillary Solution Consultant/Lead

Infinite Computer Solutions (ICS)

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Remote

Full-time

Note : GCEAD, L2EAD, consultant can apply for this position who can work on W2. Job Descriptions : Core Responsibilities: Architect solutions for inpatient (eMAR, PowerForms, PowerPlans) and specialty streams (OB module, ED triage, Perioperative).Support Materials Management, CBORD nutrition, and Clairvia staffing interfaces (FHIR, HL7) across all ancillary services.Oversee custom Discern CCL and DA2 rule development for clinical decision support, alerts, and advanced reporting.Collaborate wi
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Posted 33 days ago | Updated 12 days ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Boulder, Colorado, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 9 days ago | Updated 3 hours ago

Clinical Project Manager SME with AI/ Gen experience-Hybrid@NY

BURGEON IT SERVICES LLC

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New York, New York, USA

Third Party, Contract

Role: Clinical Project Manager SME with AI/ Gen experience Location: New York city, NY Hybrid. Long term contract Domain: Life Science Clinical R&D + Gen AI + project management Comfortable working in a matrix environment with clinical, regulatory, and tech teams.Demonstrates strong problem-solving and decision-making under tight timelines.Ability to lead and coordinate cross-functional teams from offshore and onshore.Strong stakeholder management and communication across time zones and geograph
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Posted 4 days ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Lake Success, New York, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 13 days ago | Updated 3 hours ago

Veeva Clinical Data Tester - Remote

Smart Source Technologies

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Remote

Contract

Veeva Clinical Data Management Tester Location : Fully Remote Duration : 12 months contract + extension Pay rate : $50/hr W2 (All Incl) Key requirements: Proficiency in CDMSExpertise in EDCHands-on experience in full cycle testing with Veeva
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Posted 10 days ago | Updated 5 days ago

Bidirectional Clinical Data Exchange Architect

Digital Minds Technologies Inc.

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Remote

Contract

Job Title: Bidirectional Clinical Data Exchange Architect Location: Durham, NC (Remote) Project Duration: 6+ Months Contract (Only W2 Contracts) Job Description: The Bidirectional Clinical Data Exchange Architect will be responsible for designing, implementing, and maintaining bidirectional clinical data exchange solutions. This role requires a deep understanding of healthcare interoperability, data exchange standards, and clinical workflows. Key Responsibilities: Architecture Design: Design and
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Posted 39 days ago | Updated 4 days ago

Clinical Research Coordinator

Eximia Research

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Murfreesboro, Tennessee, USA

Full-time

Job DescriptionCompany Description Eximia Research is a fully Integrated research sites network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). Our premier, multidisciplinary wholly owned research sites located across country and known for excellent trial execution, rapid subject recruitment/enrollment and delivery of a quality data. Clinical Research Coordi
Posted 8 days ago | Updated 1 hour ago