Referso Jobs

CRA II - FSP - Sponsor Dedicated

Syneos Health · Posted Nov 5, 2026

Open

Hybrid
Associate

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CRA II - FSP - Sponsor Dedicated

Syneos Health · Posted Nov 5, 2026

Open

Hybrid
Associate

Apply with RefersoAI Apply on careers page

Sr Clinical Operation Specialist / Lead Clinical Operation Specialist

Syneos Health · Posted May 13, 2026

Open

Senior
7–10 years

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Senior Clinical Operations Specialist responsible for supporting clinical trial management, budgeting, monitoring, and coordination of external service providers.

Responsibilities

Support set-up and maintenance of information in Clinical Trial Management Systems and other systems
Update data, timelines, milestones, Ethics Committee / Health Authority authorizations
Support (Sr.) CPM with study budget management
Perform Good receipt booking in line with Vendor financial report and study status
Support set-up and maintenance of Trial Master File

Skills

CTA experience centralized monitoring exposure operational understanding of clinical research communication skills fluency in English proactive resourceful quick learner CTMS

Senior Clinical Research Associate - CNS - Immunology - Germany

Worldwide Clinical Trials · Posted Nov 6, 2026

Open

Remote, Germany
Remote
Senior
3+ years

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Responsibilities

Lead site qualification, initiation, interim monitoring, management, and close-out activities in accordance with study protocols, GCP, applicable regulations, and SOPs.
Protect patient safety and data quality by reviewing informed consent, source documentation, CRFs, safety information, and protocol compliance.
Partner with investigative sites to resolve data queries, maintain regulatory and site documentation, manage investigational product accountability, and support timely, accurate study data.
Coordinate site regulatory and ethics documentation, study materials, and relevant documentation for the Trial Master File.
Serve as a Lead CRA on global studies when required, coordinating CRAs and contributing to monitoring plans, study-specific tools, templates, and visit report reviews.

Requirements

MD
Pharmacy qualification
four-year college qualification in a medical, biological, physical, health, pharmacy, or related science
two-year college qualification or equivalent education/training, preferably in nursing or life sciences
Nice to have: full-service monitoring

Skills

clinical monitoring site management

Site Activation Leader

Parexel · Posted Nov 6, 2026

Open

Remote, United States
Remote
Full-time · Mid
4–7 years

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Provide expert planning and functional oversight for clinical trial programs and individual studies, driving operational excellence and the on-time, high-quality initiation of clinical research sites.

Responsibilities

Lead site activation planning and strategy development for assigned clinical studies, overseeing milestones and deliverables from site feasibility through last site activation.
Develop, coordinate, and execute the study critical path plan, including site feasibility, site selection, Regulatory Green Light, site initiation, site activation, system setup, Trial Master File and Expected Document List management, ethics committee and regulatory authority or Ministry of Health strategy, informed consent form customization, risk mitigation, activation requirements, tools, and reporting.
Monitor and report site activation progress across multiple studies, identify potential delays and risks, and lead cross-functional teams in resolving complex activation challenges.
Provide guidance to site activation team members and serve as a liaison among project management, site start-up teams, site activation functions, and clinical operations leadership.
Manage client relationships and communications regarding site activation timelines and deliverables, and serve as the Study Start-Up Subject Matter Expert for designated client accounts.

Requirements

Bachelor's degree in Life Sciences
Healthcare

Senior Site Navigator

Fortrea · Posted Nov 5, 2026

Open

Remote, Mexico
Remote
Senior
3–5 years

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Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach through to site activation.

Responsibilities

Oversight of site level tasks associated with efficient site activation in accordance with ICH/GCP guidelines, local regulations, SOPs and project requirements
Identifying potential research sites that align with the study's criteria and assessing their capabilities and resources
Conduct initial site outreach, i.e., site engagement, collection of Confidentiality Agreement, and feasibility survey
Remote Pre-Study Visits and follow up documentation, including visit preparation, trip report completion
Support customization and translation of informed consent forms and patient-facing materials

Requirements

University/College degree (life science preferred)
certification in a related allied health profession
nursing certification
medical technology
laboratory technology

Skills

ICH/GCP RA IRB/IEC regulations

Site Navigator II

Fortrea · Posted Nov 5, 2026

Open

Remote, Mexico
Remote
Full-time · Associate
2+ years

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Coordinates site-level activities throughout the start-up phase of a clinical study, serving as the single point of contact for investigative sites to ensure smooth progression from feasibility to activation.

Responsibilities

Oversight of site level tasks associated with efficient site activation in accordance with ICH/GCP guidelines, local regulations, and SOPs
Identifying potential research sites that align with the study's criteria and assessing their capabilities
Conducting initial site outreach, collection of Confidentiality Agreement, and feasibility survey
Performing Remote Pre-Study Visits and follow up documentation
Support customization and translation of informed consent forms and patient-facing materials

Requirements

University/College degree (life science preferred)
certification in a related allied health profession
Nursing certification
Medical degree
Laboratory technology

Skills

ICH/GCP guidelines RA regulations IRB/IEC regulations clinical research contract and budget negotiation

PMO Project Manager

Sitero LLC · Posted Nov 4, 2026

Open

Remote, Poland
Remote
Full-time · Associate
2+ years

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Manages assigned projects or workstreams within established PMO standards and governance, ensuring they are planned, monitored, communicated, and delivered with discipline and consistency.

Compensation

Sitero offers a competitive compensation and benefits package, including base salary, variable pay, paid time off, and healthcare and retirement benefits.

Responsibilities

Manage projects or workstreams through all phases of the Project Life Cycle
Manage multiple concurrent client engagements
Lead the sales-to-delivery handoff for assigned clients
Set up the project in enterprise systems
Develop and maintain integrated project plans

Requirements

Bachelor’s degree in life sciences, clinical research, business administration, information technology, project management, or a related field; or an associate degree plus 2 additional years of relevant experience; or an equivalent combination of education and experience
Nice to have: CAPM
Nice to have: PMP
Nice to have: project management certification

Skills

project management clinical trial experience client-facing or client engagement

CRA II - FSP - Sponsor Dedicated

CRA II - FSP - Sponsor Dedicated

Responsibilities

Requirements

Skills

Benefits

Sr Clinical Operation Specialist / Lead Clinical Operation Specialist

Responsibilities

Skills

Senior Clinical Research Associate - CNS - Immunology - Germany

Responsibilities

Requirements

Skills

Site Activation Leader

Responsibilities

Requirements

Senior Site Navigator

Responsibilities

Requirements

Skills

Site Navigator II

Responsibilities

Requirements

Skills

PMO Project Manager

Compensation

Responsibilities

Requirements

Skills

Skills

Benefits

Benefits

Trial Master File jobs

Responsibilities

Requirements

Skills

Benefits

Responsibilities

Skills

Responsibilities

Requirements

Skills

Responsibilities

Requirements

Responsibilities

Requirements

Skills

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Skills

Benefits

Benefits