Associate Clinical Research Manager (aCRM) - Lung
New
M
Merck & Co., Inc.Clinical Research
United StatesFull-TimeMiddle
SalaryUSD 117000 - 184200 / year
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Job Details
- Languages
- English
- Experience
- 4+ years of experience in clinical research
- Required Skills
- Project Management
Requirements
- Bachelor’s degree in science or a comparable field.
- 4+ years of experience in clinical research.
- Proven experience in project management and/or site management.
- Strong knowledge of clinical trial planning, management, and associated metrics.
- Understanding of the local regulatory environment and ICH/GCP guidelines.
- Ability to work effectively in a remote or virtual environment across functions and cultures.
- Strong communication, diplomatic, and interpersonal skills for building investigator relationships.
- Demonstrated ability to drive conflict resolution and manage performance/compliance issues.
- Proficiency in written and spoken English.
- CRA experience preferred.
Responsibilities
- Serve as the main point of contact for assigned protocols, bridging the gap between Country Operations and clinical trial teams.
- Manage study timelines and deliverables, including feasibility, site selection, patient recruitment, and study execution.
- Ensure trial compliance with ICH/GCP regulations, company policies, and adverse event reporting requirements.
- Lead local study teams, providing training and coordinating activities for CRAs, CTCs, and COMs.
- Create and implement local risk management plans for assigned studies.
- Maintain accuracy in key systems including CTMS and eTMF.
- Collaborate with external vendors, investigators, and internal stakeholders such as Regulatory Affairs and Pharmacovigilance.
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