Global Study Leadership

2 days ago


Belgrade, Central Serbia IQVIA Full time

*Please note that only candidates located in the listed locations will be considered for the role

Job Overview

Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Clinical Lead is a member of the core project team responsible for the clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Clinical Leads ensure clinical delivery to customers, lead clinical teams and partner with Project Leaders and other functional teams ensuring projects meet delivery requirements at all times.

Essential Functions


• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).

• Accountable for meeting projects' recruitment targets and ensuring appropriate recruitment strategies are in place.

• Contribute to the development of the project risk mitigation plan and manage clinical risks through the project's lifecycle.

• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.

• Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.

• Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.

• Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.

• Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.

• Conduct regular team meetings and communicate appropriately to achieve objectives.

• Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.

• May contribute to the development of the clinical delivery strategy for proposals. Participate in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.

• May mentor and coach new peers as they assimilate into this role.

• May work as a primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.

• May attend site visits as applicable in support of project delivery.

Qualifications


• Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required

• Requires 5 years clinical research/monitoring experience or equivalent combination of education, training and experience.

• Requires basic knowledge of Project management practices and terminology.

• Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;

• Requires broad protocol knowledge and therapeutic knowledge.;

• Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.

• Requires understanding of project finances.

• Knowledge of clinical trials - Knowledge of clinical trial conduct in addition to skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.wnership).

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more



  • Belgrade, Central Serbia IQVIA Full time

    Job OverviewProject Management Analysts (PMA) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) providing support with project management activities to mitigate risk,...


  • Belgrade, Central Serbia 3 Years On A Rock Full time

    You've built a career you can be proud of — leading teams, achieving results, and creating impact. But now you might be wondering… what's the next chapter?If you have15+ years of professional experience, including time inleadership, management, or executive positions, and you're ready to combine your skills with more freedom, flexibility, and fulfillment...


  • Belgrade, Central Serbia PSI CRO Full time €80,000 - €120,000 per year

    We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.If...


  • Belgrade, Central Serbia IQVIA Full time

    Study Start-Up SpecialistIQVIA BiotechSerbia HomebasedJob OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance...


  • Belgrade, Central Serbia Hemofarm A.D. Full time

    Hemofarm produces high quality pharmaceutical products within the leading pharmacotherapeutic groups, observing the key corporate values: Agility, Integrity, Entrepreneurship and ONE STADA.Regulatory Global CMC ExpertPlace of work: BelgradeAbout the job:As Regulatory Global CMC Expert within the organizational unit Global Regulatory Affairs, Regulatory CMC-...


  • Belgrade, Central Serbia Syneos Health Full time

    DescriptionManager, Project Associate - RWLP ** Based in SERBIA **Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer...


  • Belgrade, Central Serbia Sowelo Consulting sp. z o.o. Full time

    Senior Analyst, Global Benefits – Work From Anywhere in Poland (B2B)Are you a Benefits Expert who gets a real kick out of making complex processes simple, automated, and globally compliant? We are partnering with a fantastic, fast-growing international client to find a Senior Analyst, Global Benefits. This is a prime opportunity to step into a strategic,...


  • Belgrade, Central Serbia IQVIA Full time

    Investigator Site Contracts ManagerHomebasedJob OverviewManage the contract strategy and support delivery of all required start-up contracting activities for selected sponsors and for complex studies or multi-protocol programs as determined by the Sponsor's requirements. This is a sponsor facing role.Essential Functions• Responsible for the development of...


  • Belgrade, Central Serbia microTECH Global LTD Full time

    The compiler team is developing an automated optimization process that adapts our unique hardware architecture to run any high-performance computing application, with little to no code modifications required. By using iterative rounds of telemetry and optimization, our compiler is able to intelligently adapt our accelerator into a workload-specific ASIC, at...

  • Senior Manager of

    4 days ago


    Belgrade, Central Serbia ZEMA Global Data US, LLC Full time

    Location: London, UK or Denver, CL  or Houston or Dallas, TX  (please kindly note, we are not accepting candidates outside this states)Position Type: Full-time, PermanentWork model: HybridIndustry: Commodities & EnergyReport To: Chief Data OfficerABOUT US:  Founded in 1995, Zema Global Data Corporation empowers organizations to simplify complexity, reduce...