Clinical Trial Manager – FSP
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Clinical Trial Manager at Parexel managing trial activities and ensuring compliance to regulations. Focusing on project management and collaboration with CROs and stakeholders.
Responsibilities:
- Accountable for trial activities for responsible R/OPU
- Verify trial compliance with GCP-ICH and regulations
- Manage and review trial budget
- Conduct trial-specific training for partners
- Oversee operational feasibility of trial timelines
- Finalize and validate site selection
- Coordinate country level engagement plans and recruitment
- Maintain oversight during clinical trial conduct
- Verify timeliness of clinical trial data cleaning
- Build and maintain engagement with Investigators and patient organizations
Requirements:
- Minimum 2+ years of regional CTM experience
- Strong clinical trial project management experience
- In-depth understanding of project management
- Experience in Therapeutic Areas relevant in client pipeline is desirable
- Familiarity with guidelines and standard of care is desirable
- Experience in working with CROs and POs is desirable
- University degree (e.g. Masters degree or comparable degree) with several years relevant experience in required area, major focus in Biomedical Life Sciences
Benefits:
- Health insurance
- Professional development
- Flexible working arrangements
Similar Jobs
Clinical Trial Manager – Project Management, Sponsor Dedicated
Clinical Trial Manager responsible for Project Management focused on patient safety and compliance in Brazil. Collaborating with teams to ensure regulatory compliance and data integrity.
Clinical Research Change Management Consultant
Clinical Research Change Management Consultant leading operational assessments and change strategies for healthcare clients. Collaborating with multi-site systems to enhance research operations.
Clinical Trial Manager
Clinical Trial Manager managing execution of clinical studies for Inogen's respiratory medical devices. Ensuring high-quality data collection and regulatory compliance across studies in a fast-paced environment.
Clinical Research Manager – Ophthalmology
Clinical Research Manager managing ophthalmology projects across various countries. Ensuring compliance with clinical trial regulations and establishing strong relationships with investigators and partners.
Clinical Scientist
Clinical Scientist role at ICON supporting respiratory clinical studies with interaction with various stakeholders. Work involves medical monitoring and data management responsibilities.
Clinical Trial Manager
Clinical Trial Manager managing clinical trial operations at ICON plc. Oversee clinical trials while ensuring compliance with regulations and quality standards.
Clinical Scientist I
Clinical Scientist conducting studies to advance understanding of new therapies at ICON plc. Designing protocols and collaborating with teams to ensure quality and efficiency.
Clinical Trial Manager
Clinical Trial Manager managing clinical operations for studies in Korea. Ensuring compliance with ICH GCP and delivering clinical outcomes within set timelines.
Principal Biostatistician, FSP
Principal Biostatistician providing statistical support for leading clinical trials in collaboration with a global pharmaceutical client. Utilizing advanced statistical methods to advance clinical development.
Clinical Trial Manager, Homebased
Clinical Trial Manager responsible for managing Phase 1 clinical research studies at Syneos Health. Collaborating with various teams to ensure successful study execution and compliance.
Principal Biostatistician, Clinical Trials
Lead life‑saving clinical research as a Principal Biostatistician at NMDP. Mentoring biostatistics team and providing statistical support for clinical trials.
Associate Director – Clinical Scientist, Cardiovascular Trials
Clinical Scientist Associate Director supporting execution of cardiovascular trials at Amgen. Collaborating across teams to ensure study quality and protocol compliance.
Clinical Trial Manager – Contract
Clinical Trial Manager managing clinical trial activities at 4D Molecular Therapeutics. Overseeing daily operations of phase 1-3 clinical trials as a remote position.
Experienced Local Clinical Trial Manager – Single Sponsor
Clinical Trial Manager overseeing site management and monitoring deliverables with focus on patient safety in clinical trials. Collaborating with teams to navigate complexities in drug development and commercialization.
Clinical Trial Manager
Clinical Trial Manager at Syneos Health managing site and clinical monitoring deliverables. Ensuring compliance, patient safety, and collaborating with cross-functional teams.
Clinical Trial Manager
Clinical Trial Manager managing clinical monitoring and site deliverables for Syneos Health, a global life sciences services organization.
Clinical Trial Manager
Clinical Trial Manager responsible for clinical trial oversight and site management at Syneos Health. Collaborating with cross-functional teams to ensure compliance and deliverables are met.
Principal Clinical Research Scientist
Principal Clinical Research Scientist driving clinical evidence strategy for diagnostics at Radiometer. Leading global clinical studies and collaborating with experts across functions.
Clinical Research Regulatory Affairs Manager
Regulatory Affairs Manager overseeing compliance for clinical operations at Sarah Cannon Research Institute. Developing strategies to ensure FDA compliance and managing relationships with sponsors and regulators.
Country/Local Clinical Trial Manager – FSP
Country Study Operations Manager managing country level activities and vendor relations for clinical trials at Parexel in Germany.