Clinical Trial Hub Safety Associate
hace 23 horas
Why Patients Need You
Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.
Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple.
Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.
What You Will Achieve
You will be relied on by the company to monitor its drug, biologics and medical devices surveillance program.
This will include intake, evaluation and processing of the adverse reports received.
You will support the clinical trial as well as the post marketing activities.
As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team.
Your focus and ability to meet team targets will help in completing important deliverables on time.
Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams.
It is your dedication and hard work that will make it possible for Pfizer's customers and patients to receive the medicines they need, when they need them.
How You Will Achieve It
- Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
- Provide oversight, team mentoring on case handling aspects, data extraction and analyses and conduct follow-up activities.
- Review, analyze, prepare, and complete safety-related reports within scope to determine the safety profile of Pfizer's products and to meet regulatory requirements.
- Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios.
- Manage, where applicable, safety resources in the local team.
- Provide specific pharmacovigilance or product knowledge and experience, as required by the business, and mentor colleagues accordingly.
- Develop and maintain advanced knowledge of all products within the Pfizer portfolio.
- Develop and maintain expertise of all assigned products, of applicable corporate policies.
- Design and oversee the tracking of applicable safety metrics.
- Manage project and process management meeting established deadlines.
- And search functions in the safety database and data mart.
**Qualifications**:
Must-Have
- Bachelor's Degree
- 3+ years' experience
- Demonstrated organizational/project management skills
- Solid knowledge of global regulations and guidelines for drug development
- Demonstrated analytical and statistical skill.
- Ability to make decisions independently and resolve issues appropriately
- Strong skills in productivity, organizational and time management in order to meet strict regulatory compliance goals
- Fluent in spoken and written English
Nice-to-Have
- Master's degree
- Relevant pharmaceutical industry experience
- Familiarity with management of performance metrics
- Ability to make decisions independently in both routine case processing and unique and/or complex situations, and to resolve issues appropriately to achieve a desired result or impact
Work Location Assignment: Flexible
EEO (Equal Employment Opportunity) & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.
Medical
LI-PFE
-
Clinical Trial Hub Safety Associate
hace 23 horas
San José, Costa Rica Pfizer A tiempo completoWhy Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary...
-
Data Safety Management Specialist
hace 1 día
San José, San José, Costa Rica Pfizer A tiempo completoPfizer's mission is to empower healthcare decisions regarding the safe and appropriate use of medicines for patients.The role of a Senior Associate in our Medical and Safety team is crucial in connecting evidenced-based medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. This involves creating frameworks...
-
Clinical Trial Solutions Specialist
hace 1 día
San José, San José, Costa Rica Clario A tiempo completoOverviewWe are united and driven by patients, committed to making a difference in the lives of individuals around the world.Job SummaryThe Clinical Trial Solutions Specialist will be responsible for delivering high-quality eCOA solutions design consultation to our pharmaceutical/biotechnology industry clients. The successful candidate will align with our...
-
Project Manager
hace 23 horas
San José, Costa Rica Clario A tiempo completoOverview:**Clario.** The Best of ERT & Bioclinica.Join Clario's San Jose, Costa Rica team as a **Project Manager** and support Cardiac Safety clinical trials.Our CS Project Manager is responsible for directing/managing services for client projects to assure high quality, on-time and on-budget services while promoting excellent customer service.- Clario...
-
Clinical Data Management Associate
hace 23 horas
San José, Costa Rica Microport Orthopedics Sa A tiempo completoAt MicroPort, we relentlessly strive to master every detail of our medical solutions to prolong and reshape patients' lives everywhere.We welcome motivated and talented people who want to join our dynamic and inclusive company, working together to deliver meaningful medical breakthroughs.To accomplish this, we hold to our core values of Quality, Integrity,...
-
San José, San José, Costa Rica Msd A tiempo completoJob OverviewWe are seeking an experienced Clinical Data Management Analyst to join our team. As a key member of our clinical operations team, you will be responsible for executing end-to-end data management activities for clinical trials.Key Responsibilities:Develop and maintain data management tools and systems to support clinical trial data management...
-
Safety Surveillance Associate
hace 24 horas
San José, Costa Rica Pfizer A tiempo completoWhy Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary...
-
Safety Data Management Specialist
hace 4 días
San José, Costa Rica Pfizer A tiempo completoWhy Patients Need You Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary...
-
Safety Data Managment Specialist
hace 23 horas
San José, Costa Rica Pfizer A tiempo completoWhy Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary...
-
Clinical Data Information Specialist
hace 7 días
San José, San José, Costa Rica Labcorp A tiempo completo**Company Overview:** Labcorp is a leading healthcare company dedicated to improving human health. Our organization operates with integrity, respect for people and the environment.As a Clinical Data Analyst at Labcorp, you will play a vital role in ensuring data quality and accuracy. This position involves collaborating with project teams to set up,...
-
Safety Data Management Specialist
hace 5 días
San José, Costa Rica Pfizer A tiempo completoWhy Patients Need You Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary...
-
Senior Clinical Operations Manager
hace 5 días
San José, San José, Costa Rica Clario A tiempo completoAbout Clario">At Clario, we deliver leading endpoint technology solutions for clinical trials. With over 19,000 clinical trials delivered in support of 870 regulatory approvals, our global team of science, technology, and operational experts has been delivering the richest clinical evidence for nearly 50 years.">Job Summary">We are seeking a highly...
-
Clinical Data Management Lead
hace 4 días
San José, San José, Costa Rica Labcorp A tiempo completoJob SummaryThis role leads studies involving healthy volunteer and patient populations, multi-site complex protocol design, and strong client management. The successful candidate will be accountable for DM deliverables, providing instruction to their study team and reviewing their output to ensure high quality.Key ResponsibilitiesEnsure all allocated...
-
Field Clinical Specialist CRM
hace 7 días
San José, San José, Costa Rica Boston Scientific Corporation A tiempo completoJob Summary:The Field Clinical Specialist CRM will play a critical role in ensuring the success of clinical trials by providing technical support and training to physicians, hospital personnel, and staff. This individual will be responsible for monitoring inventory levels, initiating logistics, and coordinating communication between internal and external...
-
Patient Safety Lead
hace 1 semana
San José, Costa Rica AstraZeneca A tiempo completo**OBJECTIVE** - Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to Patient Safety. Complete all required training on the AZ Code of Conduct and supporting Policies and Standards on time. Report potential issues of noncompliance. - Ensure and monitor...
-
Associate Eds Reviewer
hace 17 horas
San José, Costa Rica Labcorp A tiempo completo**Essential Job Duties**: - Follow applicable departmental Standard Operating Procedures and Work Instructions. - Complete required trainings according to timelines. - Review and action queries on an ongoing basis and update database appropriately in accordance with Global Data Management Plans and applicable standardized data management. - Perform UAT...
-
Project Coordinator
hace 23 horas
San José, Costa Rica Clario A tiempo completoAt Clario, we put people first, always.We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives.We value the contribution each of our people brings.It's only through our people that we can continue to innovate technology that will shape the future of clinical...
-
Solutions Design Analyst
hace 5 horas
San José, Costa Rica Clario A tiempo completoOverview:Are you ready to make a real difference?Clario-Costa Rica has a **Solutions Design Analyst opportunity**!In this role, you will take responsibility for delivering the highest quality eCOA solutions design consultation to our pharmaceutical/biotechnology industry clients.You will align with our project teams and interface with clients and Clario...
-
San José, San José, Costa Rica Pfizer A tiempo completoPfizer Worldwide Medical and Safety colleagues play a crucial role in connecting evidence-based medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.We empower healthcare decisions regarding the safe and appropriate use of medicines for patients by monitoring our drug, biologics, and medical devices...
-
Senior Clinical Data Manager
hace 6 días
San José, Costa Rica Labcorp A tiempo completo**(REMOTE) Essential Job Duties**: **- Lead studies including (but not limited to) a combination of healthy volunteer and patient populations, multi-site, complex protocol design, strong client management required or reduced timelines. Ability to organize and effectively prioritize workload and deliverables. - As the Study Manager, be accountable for all DM...