44 800 EUR

Senior Site Engagement Lead, Clinial Operations (Ref. No.: R1055592)

IQVIA RDS Slovakia, s. r. o.

Place of work
Remote work
Contract type
Total wage (gross)
44 800 EUR

Information about the position

Job description, responsibilities and duties

Senior Site Engagement Manager

Flexible locations in Europe which include Poland, Bulgaria, Hungary, Slovakia, Czech Republic, Spain, Portugal, and Italy

IQVIA™ Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers and patients. IQVIA’s Real World Evidence Solutions (RWES) group is recruiting Real World Evidence Associate Site Management Leads (ASML) who are the responsible of having the clinical oversight of a project and have a key lead role by coordinating CRAs and SMs regionally and cross-regions from the start to the close-out of the project. They are RWE Physician Initiated Data Generation experts and they apply clinical research experience and skills to engage site management/monitoring staff to ensure process and practice methodology is applied consistently and in accordance with project scope and budget, SOPs, policies, good clinical practices and applicable regulatory requirements.

Lead the planning of the Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies by applying clinical research expertise, exceptional decision making skills and innovative approaches to problem solving. Proactively set project goals and tangible expectations for SPS project team members. Develop, design and implement site engagement and patient retention strategies to real-world studies incorporating technical and innovative solutions to support these strategies.
• Develop, implement and maintain the Site Recruitment, SPS Operations and SPS Risk Management planning and assist with the project strategy planning and implementation.
• Collaborate with other functional groups within the company such as data management, quality assurance site engagement and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.
• Serve as internal consultant to project teams to implement operational site and patient engagement plans on new and/or existing projects
• Serve as primary operational project contact for site engagement and retention programs with project teams to ensure appropriate communication channels are maintained and reporting schedules adhered to as required
• Develop and deliver presentations/training to clients, colleagues and professional bodies, as required.
• Participate in business development activities such as proposal development and bid defenses.
• Maintain knowledge of current engagement and retention trends, vendors, and technologies to increase productivity and recommend additional support as needed; leverage internal intelligence to support and refine strategy
• Provide technical expertise as able in support of project specific and interdepartmental training efforts
• Support continued process improvement to ensure quality.
• May be assigned additional responsibilities as needed to support projects and other corporate/departmental initiatives.

• Knowledge of drug development processes, knowledge and ability to apply ICH/GCP/GPP and regulatory guidelines.
• Analytical skills
• Leading/supervising
• Good written and verbal communication skills including good command of English
• Effective organizational, problem solving and time management skills (ability to manage competing priorities)
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
• Ability to influence effectively within and across organizational teams and project teams including GPSS Teams, ESL, SSL, PM and the customer
• Ability to work creatively and independently in a complex global environment.
• Ability to adapt and be flexible to changing priorities
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
• System/process deployment and implementation experience a plus
• Patient and/or Site Engagement experience a plus.

Minimum required education and experience:
• Bachelor's degree, preferably in a life sciences discipline, and a recent career history of clinical monitoring experience, together with proven team leadership experience; or equivalent combination of education, training and experience.

Next Steps:

You will be contacted by one of our recruiters to arrange a prescreen call should your background be relevant for this opportunity who will be able to give you more information on this team and the opportunity and also explain the assessment process to you for this role.

Employee perks, benefits


Requirements for the employee

Candidates with education suit the position

University education (Bachelor's degree)
University education (Master's degree)
Postgraduate (Doctorate)

Educational Specialization

Medicine, Pharmaceutical, Clinical Research, Science

Language skills

English - Advanced (C1)


Brief description of the company

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

Number of employees

1000 an more employees

Company address

IQVIA RDS Slovakia, s. r. o.
Vajnorská 100/B
831 04 Bratislava - mestská časť Nové Mesto
ID: 3701452   Dátum zverejnenia: 24.6.2019