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Patient & Site Services Manager based in Bratislava
IQVIA RDS Slovakia, s. r. o.
Place of work
Zámocká 34, Bratislava region
Zámocká 34, Bratislava region
Contract type
full-time
full-time
Information about the position
Job description, responsibilities and duties
TSSU - Clinical Planning and Analytics team has an exciting opportunity for a Patient & Site Services Manager.
The person can be office based in Bratislava or home-based anywhere in the country.
Purpose:
Develop capabilities and processes through continual evaluation of existing and future needs in accordance with corporate initiatives. Responsible for providing input to study strategies for any given opportunity and collaborating with other involved Quintiles groups. May be responsible for some or all of the following activities at any one time.
Responsibilities:
Work as part of RFP (Request for Proposal) and study strategy development teams (including Therapeutic Strategy Leads, Medics, Feasibility, Strategic Site Intelligence and others) to support strategy planning / study forecasting for new studies and opportunities.
Use a variety of tools to support development of strategies by understanding study and customer requirements (per protocol information, expectations from sales team, etc.), and by mining and evaluating Quintiles' historical trial data (which countries, how many sites within each country, patient recruitment rates, etc.) specific to each unique study.
Evaluate and interpret data and then translate what the data is showing to the colleagues during strategy discussions.
Prepare post-strategy summary of data, methodology, and results to support proposals.
Provide enrollment strategy related support to study teams for bid defenses (including explanations of data and methodology, results, interpretation of results, etc.). Support handover of strategy information to study team upon award.
Produce and provide simulation results reaching beyond patient enrollment, to include outcomes projections, CRF/SDV projections.
Assist in improvement of existing tools and development of new tools to mine data, build strategies and produce advanced simulations.
May be involved in other tasks relating to recruitment and study forecasting, training and mentoring new users and strategic analysts, performing administrative tasks to support data availability and user access.
The person can be office based in Bratislava or home-based anywhere in the country.
Purpose:
Develop capabilities and processes through continual evaluation of existing and future needs in accordance with corporate initiatives. Responsible for providing input to study strategies for any given opportunity and collaborating with other involved Quintiles groups. May be responsible for some or all of the following activities at any one time.
Responsibilities:
Work as part of RFP (Request for Proposal) and study strategy development teams (including Therapeutic Strategy Leads, Medics, Feasibility, Strategic Site Intelligence and others) to support strategy planning / study forecasting for new studies and opportunities.
Use a variety of tools to support development of strategies by understanding study and customer requirements (per protocol information, expectations from sales team, etc.), and by mining and evaluating Quintiles' historical trial data (which countries, how many sites within each country, patient recruitment rates, etc.) specific to each unique study.
Evaluate and interpret data and then translate what the data is showing to the colleagues during strategy discussions.
Prepare post-strategy summary of data, methodology, and results to support proposals.
Provide enrollment strategy related support to study teams for bid defenses (including explanations of data and methodology, results, interpretation of results, etc.). Support handover of strategy information to study team upon award.
Produce and provide simulation results reaching beyond patient enrollment, to include outcomes projections, CRF/SDV projections.
Assist in improvement of existing tools and development of new tools to mine data, build strategies and produce advanced simulations.
May be involved in other tasks relating to recruitment and study forecasting, training and mentoring new users and strategic analysts, performing administrative tasks to support data availability and user access.
Requirements for the employee
Candidates with education suit the position
University education (Bachelor's degree)
University education (Master's degree)
Postgraduate (Doctorate)
University education (Master's degree)
Postgraduate (Doctorate)
Educational Specialization
Life sciences
Language skills
English - Advanced (C1)
Other knowledge
Business correspondence - Expert
Microsoft PowerPoint - Expert
Microsoft Excel - Expert
Microsoft Word - Expert
Microsoft PowerPoint - Expert
Microsoft Excel - Expert
Microsoft Word - Expert
Personality requirements and skills
Solid understanding of clinical trial operations, especially pre-award, startup and patient enrollment processes.
Operational and therapeutic experience.
Strong analytical skills and ability to quickly and accurately understand data from divergent sources to provide enrollment forecasts.
Ability to work with strong minded, experienced professionals and be comfortable challenging opinions and assumptions when appropriate.
Knowledge and ability to apply GCP / ICH and applicable regulatory guidelines.
Solid organizational skills, with ability to prioritize and quickly re-focus.
Good problem solving skills and judgment, including ability to apply critical thinking.
Excellent communication and interpersonal skills, including good command of English language, listening, comprehension and interpretation skills.
Excellent teamwork skills and customer service skills; ability to establish and maintain effective working relationships with coworkers, managers and customers (both internal and external).
Demonstrated ability to deliver results within tight timeline and with good quality.
Good presentation skills.
Strong software and computer skills, including MS Office applications and databases.
Required education and experience
Bachelor's degree in life sciences or related field and 5 years' clinical research experience, including 2 years' project management experience or project/customer leadership experience in another clinical trials function or support area; or equivalent combination of education, training and experience.
Physical requirements
Extensive use of telephone communication requiring accurate perception of speech.
Extensive use of keyboard requiring repetitive motion of fingers.
Regular sitting for extended periods of time.
Operational and therapeutic experience.
Strong analytical skills and ability to quickly and accurately understand data from divergent sources to provide enrollment forecasts.
Ability to work with strong minded, experienced professionals and be comfortable challenging opinions and assumptions when appropriate.
Knowledge and ability to apply GCP / ICH and applicable regulatory guidelines.
Solid organizational skills, with ability to prioritize and quickly re-focus.
Good problem solving skills and judgment, including ability to apply critical thinking.
Excellent communication and interpersonal skills, including good command of English language, listening, comprehension and interpretation skills.
Excellent teamwork skills and customer service skills; ability to establish and maintain effective working relationships with coworkers, managers and customers (both internal and external).
Demonstrated ability to deliver results within tight timeline and with good quality.
Good presentation skills.
Strong software and computer skills, including MS Office applications and databases.
Required education and experience
Bachelor's degree in life sciences or related field and 5 years' clinical research experience, including 2 years' project management experience or project/customer leadership experience in another clinical trials function or support area; or equivalent combination of education, training and experience.
Physical requirements
Extensive use of telephone communication requiring accurate perception of speech.
Extensive use of keyboard requiring repetitive motion of fingers.
Regular sitting for extended periods of time.
Advertiser
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 offices 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™
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 and more employees
ID: 2113324
Dátum zverejnenia: 16.6.2015
2015-06-16
lokalita: Bratislava region Pozícia: Clinical Data Manager, Clinical Research Associate, Pharmacist, Project Manager Spoločnosť: IQVIA RDS Slovakia, s. r. o.