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Local Project Manager -Up to 100.000 TL Bonus

Employer
Syneos Health
Location
Istanbul-InonuCadSumerSok, TUR
Salary
Competitive
Start date
23 Jul 2021
Closing date
21 Aug 2021

Job Details

Local Project Manager (Clinical Research Manager)
Sign-On Bonus up to 100.000 TL - only for solid experience on clinical project management
Sponsor-dedicated


Local Project Manager is a Sponsor-dedicated role that serves as the clinical functional lead, accountable for the clinical monitoring/site management delivery of assigned study(ies). The position as defined by scope provides leadership, mentoring, and technical support to the Clinical Operations team to ensure quality of deliverables and achievement of financial goals. Role also contains end to end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, Sponsor policies and procedures, quality standards and adverse event reporting requirements internally and externally.
This role could be responsible for a particular study for several countries in a cluster.

• Main Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT).
• Responsible for project management of the assigned studies: pro-actively plans, drives and tracks execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment, execution and close out.
• Accountable for performance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Sponsor policies and procedures, quality standards and adverse event reporting requirements internally and externally.
• Performs Quality control visits as required
• Leads local study teams to high performance: trains in the protocol other local roles, closely collaborates with and supports CRAs as protocol expert and coordinates activities across the different local country roles ensuring a strong collaboration
• Ensures compliance with CTMS, eTMF and other key systems in assigned studies
• Escalates as needed different challenges and issues to TA Head/CRD/CQM and or CTT (as appropriate)
• Responsible for collaboration with functional outsourcing vendors, investigators, other external partners in assigned studies
• Country POC for programmatically outsourced trials for assigned protocols.
• Serves local business needs as applicable in his/her country(If delegated can sign contracts and manage budgets)
• As a customer-facing role, this position will build business relationships and represent Sponsor with investigators• Proven knowledge in Project Management and site management.
• Proven organizational skills with demonstrated success required.
• Requires ability to make decisions independently and oversee important activities
relevant to clinical research activities according to predetermined global policies and
commitments with the support, oversight and supervision of the TA Head or CRD
• Requires strong understanding of local regulatory environment
• Strong understanding of clinical trial planning, management and metrics is essential as
well as the ability to focus on multiple deliverables and protocols simultaneously.
• Proficiency in written and spoken English and local language. The incumbent must be
competent and effective in written and verbal communication.

Experience Requirements:
• 5-6 years of experience in clinical research of which at least 4 as CRA

• Minimum 1-2 years of Project Management experience in clinical trials
• Bachelor degree in Science (or comparable)
• Preferable: Advanced degree, (e.g., Master degree, MD, PhD) preferable

We have a comprehensive benefits package and offer highly competitive remuneration.

Please be advised that due to volume of received applications, only selected candidates will be contacted back.

Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.

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