Greta Eros, Msn, Rn Email & Phone Number
@seattlegenetics.com
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Who is Greta Eros, Msn, Rn? Overview
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Greta Eros, Msn, Rn is listed as Manager, Global Patient Safety Operations at Revolution Medicines, a with 737 employees, based in Chicago, Illinois, United States. AeroLeads shows a work email signal at seattlegenetics.com and a matched LinkedIn profile for Greta Eros, Msn, Rn.
Greta Eros, Msn, Rn previously worked as Pharmacovigilance Quality Specialist - Contractor at Aveo Oncology and Clinical Data Manager at Tempus Labs, Inc.. Greta Eros, Msn, Rn holds Msn, Rn, Cnl, Registered Nursing/Registered Nurse from Rush University.
Email format at Revolution Medicines
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AeroLeads found 2 current-domain work email signals for Greta Eros, Msn, Rn. Compare company email patterns before reaching out.
About Greta Eros, Msn, Rn
Greta Eros, Msn, Rn is a Manager, Global Patient Safety Operations at Revolution Medicines. She possess expertise in clinical research, research, oncology, microsoft word, leadership and 15 more skills. She is proficient in German. Colleagues describe her as "Over the last couple of years, I have worked with Greta on two hepatocellular carcinoma clinical trials, with her in the position of Study Coordinator. These are complicated trials with many moving parts- her many tasks involve juggling obtaining patient information, chasing down lab samples, managing limited time and resources with busy physicians, following up on multitudes of paperwork to be updated... not to forget gathering the subject data, entering it into one of several computer systems, and then having someone like myself come to review her work (spending weeks pouring over every page and detail!), critique it and work with her to chase down discrepancies and make corrections, all while trying to keep me happy - and other Clinical Research Associates, like myself for other clients. When we worked together, I could see that she was receptive to my ideas and made an effort to incorporate them into her research coordinator practices. I could see that she did take to heart many of my recommendations- it was noticeable from visit to visit, and you could see visible improvement over time across the studies. Greta's position involves a heavy workload and thus requires strong multi-tasking skills, to be sure, however it also requires a method of managing the people around you in the correlating positions- managing patients, managing out, managing up, all of these are helped by having a personality that includes working well with others- keeping in mind that colleagues are all likely to have a full schedule too- so the trick is to keep your needs in the forefront of their mind, hoping that they want to work with you... Greta has the job skills including attention to detail, clarity of purpose, and time management, which are necessary to keep within tight project timelines, but it is also helpful to have excellent interpersonal skills. Greta has all of these, and performs at a high level despite only about 2yrs at SCCA. Together we have endured two separate data locks- a complicated process that can be very stressful- however Greta is passionate about the industry- which motivates her to do quality work, and she has good communication skills, as evidenced by her relationships with not only the patients & physicians, but also with the various study sponsor representatives- such as myself, and I can say that these data locks were not as miserable as others I have experienced, since we worked so well together! All of these characteristics are important in the study coordinator position, and Greta's work at Seattle Cancer Care Alliance will translate well to her future endeavors. I was very pleased with Greta's performance on these HCC trials, and with our collaboration; I would be pleased to work with her on any project in the future."
Listed skills include Clinical Research, Research, Oncology, Microsoft Word, and 16 others.
Greta Eros, Msn, Rn's current company
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Greta Eros, Msn, Rn work experience
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Pharmacovigilance Quality Specialist - Contractor
-Support development and management of Pharmacovigilance (PV) related processes and procedures;-Support PV quality event and CAPA management;-Support the development and management of Pharmacovigilance Agreements (PVA);-Manage oversight of PVA compliance; -Support PV vendor quality oversight activities; and-Other activities to support PV quality based on business needs.
Clinical Data Manager
• Manage the clinical abstraction process to construct the foundation of a growing database for cancer and other disease types• Drive accuracy, efficiency, and support the success and professional development of a team of abstractors• Act as the primary point of contact between the operations team and clinical data abstractors• Handle team requests and queries, providing clinical expertise and fielding specific abstraction questions• Work with multiple data sources and formats to support report and insight generation• Develop and maintain abstraction guidelines and rules by writing and updating SOPs• Maintain abstraction quality by developing, interpreting and tracking standards for accuracy of data• Recruit, select, train and guide new Data Abstractors• Uphold quality standards by coaching and counseling employees; planning, monitoring, and appraising abstractor performance
Clinical Nurse
Global Safety Risk Management Compliance Specialist
Drug Safety Quality Specialist
Sr. Drug Safety Operations Coordinator
• Continue to perform same responsibilities as Drug Safety Operations Coordinator in addition to completing more complex tasks• Identify and improve process efficiencies.• Manage the onboarding and provide training for new coordinator hires• Provide cross-functional training to individuals as needed within the Drug Safety department as well as from outside the department• Support the Drug Safety Project Manager with a variety of tasks
Drug Safety Operations Coordinator
• Facilitate the workflow of serious adverse event (SAE) reports for investigational and marketed products.• Intake and documentation of receipt of SAE documents• Data entry of basic fields in Drug Safety Database• Perform reconciliation with other departments, vendors, and business partners• Collaborate to maintain, develop and/or enhance departmental work procedures
Clinical Research Coordinator
Develop and implement procedures to comply with University, Food and Drug Administration, and study sponsor requirements while meeting the objectives of the study.Prepare and organize audits initiated by the sponsor, the University, and the FDA.Coordinate the care of patients on study by attending clinic visits, managing appointments, and ensuring patient safety.
Clinical Research Study Assistant
Provided general research support and assistance for the GI Research Program.Enter data from various sources into study databases.Obtain pathology tissue samples from UW and other outside institutions.Assist with research specimen tracking and coordination.Assist research study coordinators in various aspects of clinical research.
Student Helper
Prepare general use solutions. Autoclave tips/tubes/waste. Stock supplies. Wash lab ware. Assist with general upkeep of lab.
Colleagues at Revolution Medicines
Other employees you can reach at revolutionmedicines.com. View company contacts for 737 employees →
Chand Duggal
Colleague at Revolution MedicinesBoston, Massachusetts, United States
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Elaine C.
Colleague at Revolution MedicinesSouth San Francisco, California, United States
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Mark Tye
Colleague at Revolution MedicinesSan Ramon, California, United States
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Dylan Parsons
Colleague at Revolution MedicinesSan Francisco Bay Area, United States
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Fang Wang
Colleague at Revolution MedicinesSan Mateo, California, United States
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Mariela (Maru) Moreno Ayala, Phd
Colleague at Revolution MedicinesSan Mateo, California, United States
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Michele Famularo
Colleague at Revolution MedicinesNew York City Metropolitan Area, United States
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Emily Tonogai
Colleague at Revolution MedicinesRedwood City, California, United States
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Victoria Woodland
Colleague at Revolution MedicinesCary, North Carolina, United States
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Yi Yi
Colleague at Revolution MedicinesSan Francisco Bay Area, United States
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Greta Eros, Msn, Rn education
Msn, Rn, Cnl, Registered Nursing/Registered Nurse
Bachelor’S Degree, Bachelor Of Science In Biology
Associate’S Degree
High School
Frequently asked questions about Greta Eros, Msn, Rn
Quick answers generated from the profile data available on this page.
What company does Greta Eros, Msn, Rn work for?
Greta Eros, Msn, Rn works for Revolution Medicines.
What is Greta Eros, Msn, Rn's role at Revolution Medicines?
Greta Eros, Msn, Rn is listed as Manager, Global Patient Safety Operations at Revolution Medicines.
What is Greta Eros, Msn, Rn's email address?
AeroLeads has found 2 work email signals at @seattlegenetics.com for Greta Eros, Msn, Rn at Revolution Medicines.
Where is Greta Eros, Msn, Rn based?
Greta Eros, Msn, Rn is based in Chicago, Illinois, United States while working with Revolution Medicines.
What companies has Greta Eros, Msn, Rn worked for?
Greta Eros, Msn, Rn has worked for Revolution Medicines, Aveo Oncology, Tempus Labs, Inc., Northwestern Memorial Hospital, and Seagen.
Who are Greta Eros, Msn, Rn's colleagues at Revolution Medicines?
Greta Eros, Msn, Rn's colleagues at Revolution Medicines include Chand Duggal, Elaine C., Mark Tye, Dylan Parsons, and Fang Wang.
How can I contact Greta Eros, Msn, Rn?
You can use AeroLeads to view verified contact signals for Greta Eros, Msn, Rn at Revolution Medicines, including work email, phone, and LinkedIn data when available.
What schools did Greta Eros, Msn, Rn attend?
Greta Eros, Msn, Rn holds Msn, Rn, Cnl, Registered Nursing/Registered Nurse from Rush University.
What skills is Greta Eros, Msn, Rn known for?
Greta Eros, Msn, Rn is listed with skills including Clinical Research, Research, Oncology, Microsoft Word, Leadership, Microsoft Office, Powerpoint, and Clinical Trials.
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