About this opportunity
Integrated Resources Inc. lists this Senior Clinical Study Manager opportunity in woodcliff lake, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Provide operational leadership for assigned trials executing them on time and within budget
Overall coordination and management of clinical trials from startup to closeout
Liaise with other functional areas to identify issues, evaluate and make sound business decisions and ensure implementation of timely solutions.
Identify and select high-quality clinical vendors in conjunction with the appropriate team members
Work with the contracting/budgeting team to ensure that vendor responsibilities and payment terms are clearly defined.
Manage and effectively provide oversight of assigned clinical vendors and functional service providers to ensure data integrity and adherence with regulatory requirements.
Assure that team is receiving high quality, on time deliverables from internal and external vendors.
Collaborate with other team members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed consent documents, study management plans and final clinical study reports.
Work with finance manager on financial aspects of the project(s), including milestone payments, and monthly pass through invoices
Lead or facilitate teleconferences with internal or external group.
Oversee Clinical Trial Coordinator for assigned project to ensure successful management of project(s), including development of the project plan, maintenance of trackers, and generation of metrics reports
Assume co-monitoring responsibilities as needed.
Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to proactively recognize problem situations and work with other team members as required to resolve issues
Manage the publication process in conjunction with the publications team to assure that submission timelines are met.
Monitor and report clinical trial status using standard and adhoc review & reporting procedures and identify issues that affect functions. Ensure that each function is accountable for their deliverables.
In collaboration with Project Management and utilizing various tracking mechanisms, manage clinical trial project milestones and budget. Proactively identify issues and escalate to appropriate managers.
REQUIREMENTS:
At least 10 years of experience in the management of clinical trials, significant knowledge of overall clinical drug development and general clinical research operations in Big Pharma.
Ability to manage multiple projects simultaneously with strong organizational and planning skills.
Well-developed analytical and problem solving skills. Communicates issues to Director with action plans for resolution.
Knowledgeable in all required regulatory and compliance standards and guidelines including ICH-GCP.
Ability to effectively work with teams and promote collaborations. Exceptional interpersonal skills including the ability to influence negotiate and resolve conflicts.
Excellent verbal and written communication skills and the ability to interact with all levels of management within the organization and to external business contacts. Experience using the Inform database, PowerPoint and Excel software.
Independent judgment and decision making skills with respect to functional responsibilities. Innovative and motivated in optimizing clinical operations processes to meet deliverables.
Minimum BS or BA in related field; focusing on biological science or nursing preferred or equivalent. Advanced Degree preferred
Qualifications
10 years of experience in the management of clinical trials
Additional Information
All your information will be kept confidential according to EEO guidelines.
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Worksite address
woodcliff lake, NJ, 07677, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.