-
Senior Marketing Manager, Orthopedics, LATAM
há 3 semanas
CONMED Corporation BrasilPURPOSE · We are seeking a Senior Manager Marketing who will have Latin America (LATAM) responsibility for the growth of innovative products in the Orthopaedic portfolio. In this critical position, you will represent LATAM while partnering with the International & US based globa ...
-
Central Monitor School
há 2 horas
IQVIA Brazil, Brasil Tempo integralJob Description Summary Job Overview Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies ...
-
Clinical Research Coordinator
há 1 semana
IQVIA Brazil, Brasil Tempo integralAre you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research ...
-
Clinical Trials Assistant 1
há 5 dias
IQVIA Brazil, Brasil Tempo integralJob Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions · • Assist Clinical Research Associates (CRAs) and Regu ...
-
Clinical Research Coordinator
há 1 semana
IQVIA Brazil, Brasil Tempo ParcialAre you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research ...
-
Clinical Research Coordinator
há 1 semana
IQVIA Brazil, Brasil Tempo integralAre you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research ...
-
Field Clinical Representative
há 6 dias
BOSTON SCIENTIFIC Brazil, Brasil Tempo integralAdditional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some ...
-
IQVIA Brazil, Brasil Tempo integralOverview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in breadth and depth of Clinical Outcomes Assessment (COA) and Patient Rep ...
-
Field Clinical Representative
há 5 dias
BOSTON SCIENTIFIC Brazil, Brasil Tempo integralAdditional Location(s): N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some ...
-
Contract Negotiator
há 2 horas
IQVIA Brazil, Brasil Tempo integralJob Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor's requirements. Essential Functions · • Develop Coordinate the dev ...
-
Operations Specialist 1
há 2 dias
IQVIA Brazil, Brasil Tempo integralJob Overview Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and inter ...
-
Site Activation Coordinator in Brazil
há 5 dias
IQVIA Brazil, Brasil Tempo integralAs a Site Activation Coordinator, you'll perform tasks at a country level (for the North American team) associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and ...
-
Site Activation Coordinator
há 2 horas
IQVIA Brazil, Brasil Tempo integralJob Overview: Contract and budget negotiation with reserch site [investigator contracts]; contract amendment negotiation; TMF update; system update; tracker update Under general supervision, perform tasks at a country level associated with site activation activities in accordance ...
-
Consultant
há 2 horas
IQVIA Brazil, Brasil Tempo integralJob Overview Support business development approach for the Consulting team, preparing proposals and following up identified opportunities Essential Functions Close support to Consulting Principals on developing proposals: · • Participate with Principals on customer meetings and ...
-
Information Security Project Manager
há 5 dias
IQVIA Brazil, Brasil Tempo integralRole As Information Security Project Manager at IQVIA, you will play a critical role in safeguarding our digital assets, ensuring the confidentiality, integrity, and availability of sensitive information. You'll lead manage security programs, and drive compliance with industry st ...
-
Business Intelligence Analyst
há 2 dias
IQVIA Brazil, Brasil Tempo integralJob Overview Perform project management, research, analysis, and report preparation on a wide range of projects. Assignments typically involve evaluating customer and competitor marketplaces through primary and secondary research activities as well as analysis of company performa ...
-
Pharmacovigilance Specialist
há 1 dia
IQVIA Brazil, Brasil Tempo integralThe Pharmacovigilance team is aiming to provide expertise to the project applying their knowledge in intake adverse event cases. Your responsibilities will include: · Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and pr ...
-
Contracts Analyst 1
há 2 horas
IQVIA Brazil, Brasil Tempo integralThe Global Business Operations (GBO) team is a dynamic group with high visibility within IQVIA. GBO develops strategic proposals and budgets for our customers, and upon award, drives contract execution, including changes throughout the study lifecycle, by working with numerous in ...
-
Medical Information Specialist
há 1 dia
IQVIA Brazil, Brasil Tempo integralMedical Information Specialist IQVIA Safety Operations team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse te ...
-
Linguistic Validation Junior Project Manager
há 2 horas
IQVIA Brazil, Brasil Tempo integralJunior Project Manager Linguistic Validation Job Overview IQVIA is currently looking to expand our Translations Services team in the United States due to continued growth and demand for Linguistic Validation & eCOA services. We are currently seeking a Project Manager to join our ...
Manager, Clinical Operations - Brazil, Brasil - IQVIA
Descrição
Unleash Your Potential It takes curiosity and intellectual courage to accomplish great things. It takes brave minds to bring powerful ideas to reality and transform healthcare. We are a diverse, global team that shares a passion for collaboration and solving complex problems. Together, we help customers drive healthcare forward. Join IQVIA and see where your skills can take you.Our team would like to consider candidates with current or recent line management, managing teams in North America and Latin America.
Candidates must have past CRA experience. Applicants must be fluent in English, both written and verbally. Please submit English version of CV/Resume. This position offers the flexibility to work from home. If you DO NOT have any line management or CRA experience, please do not apply.BASIC FUNCTIONS:
Works with Clinical Operations Management staff to ensure the successful management, performance, and career development of Lead Clinical Research Associates (CRAs) and Clinical Research Associates (CRAs).
Provides training and consultation related to clinical operating activities in the conduct of clinical trial projects. Serves as a source of clinical research expertise for IQVIA Biotech clinical staff. Contributes to, and participates in, the marketing of IQVIA Biotech services.Assures compliance with Good Clinical Practices (GCPs), ICH, Standard Operating Procedures (SOPs), Working Practices (WPs), and policies and procedures set forth by IQVIA Biotech and its clients.
ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:
Clinical Staff Line Management Duties/Responsibilities:
Line management for assigned Lead CRAs and CRAs (both office and regionally based) in the following areas:
Plans career development of staff.
Anticipates resource issues and plan remedial action.
Communicates with the CTMs and/or Lead CRA, as needed, to ensure correct monitoring resources per project.
Liaise with Project Managers to ensure monitoring deliverables/targets are met, ensure project hours are met, ensure excessive total hours are noted and action taken as necessary.
Ensures any project issues and results of discussions with Project Managers and are escalated appropriately.In coordination with the Director, Clinical Operations ensures proper allocation of Operations resources.
Assesses training requirements for monitoring staff.
Organizes appropriate training in liaison with the IQVIA Biotech e-process and Integration (Training) Department. Monitors and records subsequent performance to assess the effects of training on efficiency.
Conducts field evaluation visits with staff at sites.
Holds regular one-on-one meetings with staff to discuss performance.
Writes and delivers performance appraisals.
Reviews and approve time sheets and expense reports as required.
Coach, train, and support direct reports:
Provides staff with expert clinical research and therapeutic advice.
Assists with organizing and conducting Lead CRA, CTM and CRA Staff Meetings at regular intervals.
Addresses issues discovered at meetings.
Maintains an awareness of company policies to effectively represent the company perspective to clinical staff.
Identifies training needs and ensure staff participation during in-house training activities as required.
Collaborates with Director, Clinical Operations to develop and administer an effective orientation/on-boarding process for new CTM, Lead CRA and CRA hires.
Maintains awareness of overall development in the field of clinical research and ensures that staff remains current on clinical monitoring developments.
Clinical Operations Department Duties/Responsibilities:
Assists Clinical Operations Management with review and revision of departmental SOPs, working practices, and policies.
Assists Clinical Operations Management with interviewing and making hiring recommendations and/or decisions on new staff.
Communicates staff increase and equipment needs to Director, Clinical Operations.
Communicates staff training needs to Director, Clinical Operations.
Assists Director, Clinical Operations to create and deliver new department initiatives, improvement plans or training
Assists Director, Clinical Operations with development of strategic departmental goals which correlate with corporate goals and formalize departmental action plans to meet those goals.
Assists in developing department budget and is accountable for the profit/loss and the overall financial performance of the Clinical department.
Assists Director, Clinical Operations with Process Improvement Plans and other special projects as required by the department.Provides clinical management oversight of clinical projects to ensure consistent on-time completion of client deliverables and timely escalation and resolution of issues.
Collaborates with other department and/or functional groups to ensure consistency of processes.Project Duties/Responsibilities:
May serve as CTM for projects as directed.
Assists CTMs with defining the scope of work with the clinical monitoring team.
Assists CTMs with identifying changes in scope.
Provides vacation coverage for CTMs as required.
Provides clinical expertise to project team as needed.
Business Development Duties/Responsibilities:
Participate in the development of the clinical portion of client proposals including preparation of clinical project budget and text.
Preparation for and attendance at capabilities and bid defense meetings.Participate in marketing activities, client presentations, and proposal development.
Participate in and/or attend professional and industry meetings as a representative of IQVIA Biotech.
KNOWLEDGE, SKILLS &
ABILITIES:
Thorough knowledge of clinical research process, including working knowledge of all functional areas of clinical trial management.
Strong communication skills (verbal and written) to express complex ideas.
Excellent organizational and interpersonal skills.
Positive attitude and ability to interact with all levels of staff.
Ability to balance needs of the organization with needs of staff.
Ability to protect confidential/sensitive information.
Ability to manage multiple priorities within the department and across staff.
Ability to reason independently for assessing and recommending specific solutions in clinical settings.
Ability to mentor and train clinical staff.
Understanding of basic data processing functions, including electronic data capture.
Working knowledge of Word, Excel, and Power Point.
Working knowledge of current ICH/GCP guidelines and applicable country specific regulations.
Able to qualify for a major credit card.
Valid driver's license; ability to rent automobile.
Willingness and ability to travel domestically and internationally as required.
MINIMUM RECRUITMENT STANDARDS:
BS/BA (or equivalent) in a life sciences program or RN/BSN (or equivalent) with a minimum of 8 years direct experience in clinical studies or equivalent level of education, training and experience.
Understanding of the entire clinical research process mandatory.Previous experience in personnel management within a clinical research environment preferred.
At least 5 years as a Clinical Research Associate/Clinical Monitor, prefer at least 4 years as a successful Lead CRA/Clinical Trial Manager.
Demonstrated ability to lead and motivate a group of clinical research personnel.Excellent organizational, communication (verbal and written), and interpersonal skills.
Ability to work independently, prioritize and function effectively within a matrix team environment.
Working knowledge of Word, Excel, and Power Point.
Prior global/multi region trial management experience is required.
Prior proposal development and bid defense participation is preferred.
Prior budget development and management experience is preferred.
Prior experience in electronic data capture (EDC) is preferred.
Prior site management experience is required.
Prior project team leadership/management is required.
#LI-Remote #LI-RW1 IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
