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Manager, Clinical Data Management in a CRO - Full Time REMOTE, some travel

Elan Solutions LLC · Remote — United States

Télétravail
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Résumé du poste

Lieu
Remote — United States
Mode de travail
Télétravail
Type de contrat
Temps plein
Date de publication
12 oct. 2026
Dernière vérification à la source
12 oct. 2026
Source de l'offre
via Himalayas

Missions

• Provide data management expertise to project teams, clients, and CROs, including study startup documents, data cleaning, DCF/query tracking, database QC, and SAE/AE reconciliation. • Oversee development of specifications for eCRFs/CRF, edit checks, electronic data handling, manual review, and User Acceptance Testing. • Conduct cross-functional data reviews, identify issues, and track resolutions. • Innovate and implement new technologies for process improvements. • Ensure adherence to quality control procedures. • Write and update SOPs/training guidelines. • Facilitate internal study team, client, and CRO meetings. • Review study data quality, provide metrics, and report out-of-scope activities. • Manage timelines and resources to meet deadlines. • Identify and recommend solutions for process inefficiencies. • Assist in preparing proposals and budgets for new and ongoing projects. • Direct and manage team members, including training, resource assignment, and performance reviews.

Profil recherché

• 12+ years of hands-on data management experience. • 6-7 years of managerial experience, managing a team of at least 5 people. • 4+ years of experience in the CRO environment. • Excellent oral and written communication skills. • Ability to work in the PST time zone (flexible). • Willingness to travel 2-3 times a year when necessary.

Compétences

Visa et relocalisation

L'annonce indique qu'aucun visa n'est parrainé.

L'annonce ne mentionne pas de relocalisation.

Description du poste

Job Description / Summary The Manager, Clinical Data Management is a full-time exempt position reporting to the Director, Clinical Data Management. PLEASE NOTE: Candidates must have a valid Green Card or U.S. citizenship. No visa sponsorship is available now or in the future. Must Have • 12+ years of hands-on data management experience. • 6-7 years of managerial experience, managing a team of at least 5 people. • 4+ years of experience in the CRO environment. • Excellent oral and written communication skills. • Ability to work in the PST time zone (flexible). • Willingness to travel 2-3 times a year when necessary. Responsibilities • Provide data management expertise to project teams, clients, and CROs, including study startup documents, data cleaning, DCF/query tracking, database QC, and SAE/AE reconciliation. • Oversee development of specifications for eCRFs/CRF, edit checks, electronic data handling, manual review, and User Acceptance Testing. • Conduct cross-functional data reviews, identify issues, and track resolutions. • Innovate and implement new technologies for process improvements. • Ensure adherence to quality control procedures. • Write and update SOPs/training guidelines. • Facilitate internal study team, client, and CRO meetings. • Review study data quality, provide metrics, and report out-of-scope activities. • Manage timelines and resources to meet deadlines. • Identify and recommend solutions for process inefficiencies. • Assist in preparing proposals and budgets for new and ongoing projects. • Direct and manage team members, including training, resource assignment, and performance reviews. Education and Experience Requirements • 12 years of hands-on data management experience. • 6-7 years of managerial experience, managing a team of 5+ people. • B.S./B.A. in a science or technical discipline with 8 years of data management experience, or MS degree with 6 years of data management experience; minimum 4 years in the Pharmaceutical/Biotechnology industry or CRO environment. • Proficiency in SQL or SAS is desirable but not required. • Experience with various data collection and EDC systems. Knowledge & Skills Requirements • Excellent oral and written communication skills. • Ability to work collaboratively in a multi-disciplinary environment. • Good knowledge of FDA, EMA, ICH guidelines, and GCPs, especially related to data handling and processing. Salary and Benefits • Market rate compensation as base salary with all the benefits. Originally posted on Himalayas Clinical-Data-Manager, Data-Management-Manager, Clinical-Data-Management-Senior-Manager, Clinical-Data-Analyst, Clinical-Research-Manager, Senior-Manager-Clinical-Data-Management
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