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The Clinical Trial Manager II is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical monitoring deliverables of clinical trials. This includes but is not…
Project Manager II leading Phase I-III clinical trials end to end (initiation through closure) at a dermatology/rheumatology CRO — owning budgets, timelines, vendors, sponsor communication, and cross-functional teams. Home-based anywhere in Poland; core know-how is GCP/ICH standards and clinical project management.
The Project Manager II oversees the end-to-end execution of early-phase clinical trials, managing study budgets, timelines, vendor relationships, and regulatory compliance. This role requires extensive experience in clinical research operations and strong communication skills to coordinate between sponsors, internal teams, and clinical sites.
Senior Project Manager at Indero, a dermatology/rheumatology-focused contract research organization, leads global Phase III clinical trials end-to-end from Romania as a home-based role — serving as the primary sponsor contact while managing budgets, timelines, vendors, quality, and cross-functional project teams. Requires 7+ years of clinical project management experience and strong GCP/ICH knowle
The Project Manager II oversees the end-to-end execution of clinical trials, managing budgets, timelines, and cross-functional teams to ensure regulatory compliance. This home-based role requires extensive experience in clinical trial management and strong communication skills to serve as the primary sponsor contact.
Due to ongoing global expansion, Indero is looking to hire a Regulatory Affairs Specialist. In this position, you will be responsible for preparation and submission of part I and/or part II following EU CTR and other…
The Clinical Trial Manager II (CTMII) is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical operations deliverables of clinical trials. This includes…
The Project Manager II oversees the end-to-end lifecycle of clinical trials, managing budgets, timelines, and cross-functional teams to ensure regulatory compliance. This role acts as the primary sponsor contact and requires expertise in dermatology or rheumatology research.
Leads end-to-end delivery of dermatology and rheumatology clinical trials at Indero, a contract research organization — managing budgets, timelines, sponsors, vendors, and core project teams. A remote, home-based role requiring Phase I-III trial PM experience with GCP/ICH knowledge, open only to those legally able to work in Romania.
Leads Phase I-III multisite clinical trials end to end at a mid-size CRO: study start-up, budgets, timelines, vendors, quality/risk, and sponsor communication. Requires GCP/ICH and FDA/Canadian regulatory knowledge; remote from anywhere in Canada with occasional Montreal office visits.
Indero, a dermatology-focused contract research organization (CRO), is hiring a home-based Senior Project Manager in Germany to lead multi-site Phase II–III dermatology/rheumatology clinical trials — owning sponsor communication, budgets, timelines, quality, and project teams. Requires 7+ years industry experience, GCP/ICH knowledge, and legal work rights in Germany.
Senior Project Manager at Indero, a dermatology/rheumatology-specialized contract research organization, leading global Phase III clinical trials from a home-based role open across Poland. Manages sponsor relationships, budgets, timelines, vendors and cross-functional study teams. Requires ~7+ years clinical project management experience, GCP/ICH knowledge and fluent English.
Indero, a dermatology and rheumatology-focused contract research organization (CRO), is hiring a remote USA-based Senior Project Manager to run global clinical trials end to end — acting as the sponsor's primary contact while owning planning, budgets, timelines, vendors, quality, and team leadership across all study phases.
Manages Phase I and II clinical trials by overseeing budgets, timelines, vendors, and regulatory compliance (GCP). Coordinates study start-up, TMF maintenance, and stakeholder communication using Microsoft Office.
Manages clinical research projects end-to-end, ensuring compliance with budgets, timelines, and regulations while coordinating cross-functional teams and vendors.
The Clinical Trial Delivery Trainer is responsible for developing, maintaining, coordinating, delivering, and continuously improving training programs and repositories for new and existing employees across all key…
Oversees clinical research projects, ensuring compliance with budgets, scope, and timelines while coordinating teams, vendors, and stakeholders in a CRO setting.
Project Manager I at Indero, a dermatology/rheumatology CRO, runs clinical research studies day to day — planning, budgets, timelines, site activation, vendor and sponsor coordination — under senior supervision and in line with GCP/ICH and regulatory requirements. Remote within Europe.
The Associate Director, Project Management is responsible for providing senior leadership and line management oversight for Project Management function. This role is accountable for ensuring consistent, high-quality…
The Clinical Trial Manager (CTM) is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical operations deliverables of clinical trials. This includes but is…
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