Clinical Trial Manager II

Innovaderm Research Inc.

Clinical Trial Manager II overseeing clinical monitoring activities and site performance at Indero, a CRO in dermatology. Requires extensive clinical research experience and strong regulatory knowledge.

Posted 6/3/2026full-timeRemote • 🇺🇸 United StatesSeniorLeadWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

clinical monitoringquality controlsource data verificationclinical researchLead CRAClinical Team LeaderICH standardsGCP standardsregulatory requirementsclinical monitoring plan

Soft Skills

leadershiporganizational skillstime managementmulti-taskingjudgementproblem-solvingrelationship buildingcommunication

Tools & Technologies

Microsoft OfficeWordExcelPowerPoint

Industry Keywords

biotechnologypharmaceuticalcontract research organizationCROdermatologySOPsquality assuranceproject managementclient meetingsproposal defense

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Ensures that clinical monitoring activities are performed to the Sponsor’s satisfaction, ensuring timely quality deliverables and in accordance with applicable standard operating procedures (SOPs), regulations, good clinical practices and study-specific requirements;
Identifies quality issues and trends related to site performance and clinical monitoring activities through project meetings, site communications, site visit reports and follow-up letters, quality control visits, and quality assurance audit findings. Summarizes findings and establishes action plans to bring corrective actions;
Serves as a point of contact for CRAs and Lead CRAs for assigned projects;
Provides mentoring/oversight of CRAs and Lead CRAs;
Performs site visit report review for assigned projects and tracks site visit report metrics to ensure compliance;
Contributes to the development of the Clinical Monitoring Plan;
Prepares and conducts project-specific training for the CRAs;
Develops the annotated site visit reports and monitoring tools such as source data verification worksheets;
Conducts quality control visits with CRAs;
Coordinates and leads CRA meetings;
Performs co-monitoring visits with CRAs;
May be involved in business development activities (client meetings, proposal defense meetings, requests for proposals (RFPs) requests for information (RFIs)).

Requirements

What you’ll need

B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience;
At least 8 years of clinical research experience including prior monitoring experience and at least 2 years of experience acting in a Lead CRA or Clinical Team Leader role in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry;
Strong knowledge of ICH/GCP standards and applicable regulatory requirements;
Excellent mastery of Microsoft Office suite (Word, Excel, Power Point);
Ability to work in a fast-paced evolving environment and establish good relationships with colleagues, sites and sponsors;
Excellent leadership, organizational, time management and multi-tasking skills;
Excellent judgement and problem-solving skills;
Occasional travel (up to 10% of the time), including some travel outside of the country once possible;
Fluent in English (excellent oral and written);
Experience in a CRO and in dermatology an asset.

Benefits

Comp & perks

Flexible work schedule / work schedule : Home-based position