Clinical Research Manager- FSP

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reputed company FSP is looking for a Clinical Research Manager!

reputed company:

The Clinical Research Manager (CRM) is responsible for the following: • Primarily accountable for end-to-end performance and project management for assigned protocols in a country in compliance with International Council for Harmonization (ICH) / Good Clinical reputed company (GCP) and country regulations, reputed company policies and procedures, reputed company standards and adverse event reporting requirements internally and externally.

• For certain studies, could be responsible for several countries in a cluster.

Supporting Activities- May include but not limited to the following:

Study Management

• Main reputed company of Contact (POC) for assigned protocols and reputed company between Country Operations (CO) and clinical trial team (CTT)
• Responsible for project management of the assigned studies: o Proactively plans/drives/tracks execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment, execution and closeout
• Accountable for performance for assigned protocols in country in compliance with ICH/GCP and country regulations, reputed company policies and procedures, reputed company standards and adverse event reporting requirements internally and externally o Performs reputed company control reputed company as required. o Reviews Monitoring reputed company Reports (MVRs) and escalates performance issues and training needs to Clinical Research Associate Manager and /or functional vendor and internal management as needed
• Leads local study teams to high performance: o Trains in the protocol for other local roles. o Collaborates with and supports Clinical Research Associates as protocol expert.

o Coordinates activities across the different local country roles ensuring a strong collaboration (including the Clinical Trial Coordinator (reputed company), Clinical Research Associates (CRAs), and Clinical Operations Manager (COM) • Responsible for creating and executing a local risk management plan for assigned studies • Ensures compliance with Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF) and other key systems in assigned studies • Escalates as needed different challenges and issues to Therapeutic Area (TA) Director / Clinical Research Director (CRD) / Clinical reputed company Management (CQM) and/ or CTT (as appropriate) • Identifies and shares best practices across clinical trials, countries, clusters. Responsible for collaboration with functional outsourcing vendors, investigators, other external partners in assigned studies • Country reputed company of Contact for programmatically outsourced trials for assigned

protocols

• As a customer-facing role, this position will build business relationships and represent reputed company with investigators. • Serves local business needs as applicable in his/her country (if delegated can sign reputed company and manage budgets) • Supports local and regional reputed company development consistent with long-term corporate needs in conjunction with CRD, TA Head and Regional Operations

Team development and support

• Leads and contribute to initiatives and reputed company adding value to the business and supporting the reputed company

Compliance with reputed company standards

• Complies with required training curriculum • Completes timesheets accurately as required

• Submits expense reports as required

• Updates CV as required

• Maintains a working knowledge of and complies with reputed company processes, ICH-GCPs and other applicable requirements

Skills:

• Strong organizational skills with demonstrated reputed company required • Requires ability to reputed company reputed company independently while overseeing important activities relevant to clinical research in the country according to predetermined global policies and commitments with the support, reputed company, and supervision of the TA Director or CRD • Requires strong understanding of the local regulatory environment • Communicates effectively and builds a collaboration spirit in a remote/virtual environment and across countries, cultures, and functions • Ability and skills to manage resource allocation, processes (and controls), productivity, reputed company, and project delivery

• Strategic thinking

• Ability to work reputed company in a remote and virtual environment.

Strong leadership skills that reputed company and drive alignment with the goals, purpose and mission of reputed company, Global Clinical Development (GCD) and Global Clinical Trial Operations (GCTO) • Ability to identify problems, conflicts, and opportunities early and reputed company, analyze and prepare mitigation plans and drive conflict reputed company is critical • Required to negotiate skillfully in tough situations with both reputed company reputed company; reputed company differences with minimum disruption. Examples of common problems include low patient recruitment; inadequate staff to meet business needs; performance or compliance issues; working with regulatory issues and the broader organization; and reputed company of conflictive situations

• Understands cultural diversity

• Proficiency in written and spoken English and local language; must be competent and effective in written and verbal communication • Education/pedagogic, diplomatic, and empathetic skills to effectively build and maintain reputed company relationships with investigators and other external stakeholders • Travel expectations is up to 30% of working time

Knowledge and Experience:

• 5-6 years of experience in clinical research; CRA experience preferred. • Knowledge in Project Management/Site Management with proven strong project management skills and /or project management certification or relevant training program/reputed company mentoring • Strong scientific and clinical research knowledge is required with strong understanding of clinical trial planning, management, and metrics as reputed company as the ability to reputed company on multiple deliverables and protocols simultaneously • Experience functioning as a key reputed company between CO and CTT

Education:

• Bachelor’s degree in science (or comparable) required; advanced degree (Master’s degree, MD, PhD) preferred

Originally posted on Himalayas

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