Kelly Hall Email and Phone Number
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Kelly Hall personal email
As Associate Director of Clinical Operations at Orasis Pharmaceuticals, I lead and direct the delivery of clinical trials for the groundbreaking CSF-1 presbyopia correction therapy. With 11 years of ophthalmology research experience, I have worked on drug and device trials for a variety of eye conditions, including cataract, refractive, dry-eye, glaucoma, and corneal disease.My core competencies include overseeing clinical trial execution, managing multiple clinical trial teams, providing site and vendor oversight, ensuring data quality, and meeting budget and timeline targets. I also enjoy teaching sites and team members how to think critically and strategically about clinical research, and enhancing customer experiences with integrity, care, and commitment. My goal is to advance the field of ophthalmology and improve the lives of patients with vision problems.Eye care, Eyecare, Ophthalmology, Pharmaceuticals, Medical Device, Clinical Trials, Regulatory Affairs, Drug Development, Medical Affairs, Clinical Operations, Project Management, Clinical Research, Data Analysis, Compliance, FDA Regulations, Budget Management, Strategic Planning, Clinical Trial Management, Cross-functional team leadership, Leadership, Collaboration, Adaptability, Communication, Decision-making, Problem-solving, Process, Improvement, Risk Assessment, Protocol amendments, Negotiation
Orasis Pharmaceuticals
View- Website:
- orasis-pharma.com
- Employees:
- 85
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Associate Director Medical AffairsOrasis PharmaceuticalsOmaha, Ne, Us -
Associate Director Clinical OperationsOrasis Pharmaceuticals Aug 2022 - PresentPonte Vedra Beach, Florida, UsActing Head of Clinical Operations for Qlosi approval. Provided leadership and direction to support the Orasis CSF-1 clinical trials. Responsible for the delivery of clinical trials by effectively directing and overseeing the activities of Orasis’ industry partners. -
Commercial Operations: Marketing And Strategy PreceptorshipOrasis Pharmaceuticals Aug 2022 - Jul 2024Ponte Vedra Beach, Florida, UsGained exposure to a broad range of marketing strategies and initiatives to strengthen commercial knowledgePartnered with cross-functional disciplines (marketing, medical affairs, CMC, etc.) along with external partners/advisors to contribute to strategic, best in class professional promotion, social media campaigns, and medical educationSupported the development and delivery of key messaging to defined stakeholders, including KOLs and external advisorsSupported the creation and refinement of comprehensive training content for internal use -
Senior Manager, Us Clinical OperationsOrasis Pharmaceuticals Jan 2022 - Aug 2022Ponte Vedra Beach, Florida, UsParticipate in the identification and recruitment of Investigators and assist in the development of subject recruitment strategies and start up materials.Develop relationships with study sites and Investigators through routine site contact and visits.Assist in developing key study documents (study protocol, site monitoring plan, training materials).Provide oversight of external vendors (CRO, QA, Data Management and Stats).Play a key role in identifying trends and protocol deviations across sites and study; assist with the accurate categorization and documentation of their related outcomes and actions. -
Clinical Trial ManagerOrasis Pharmaceuticals Nov 2020 - Jan 2022Ponte Vedra Beach, Florida, UsServe as Orasis brand ambassador to our clinical sites and CRO. Ensure everyone who interacts with me feels like they are treated like family.Contribute to the creation and finalization of relevant study documents such as study protocol, Investigator's Brochure, CSR, and clinical sections of regulatory documents.Provide oversight of the study sites from site selection and contract negotiation to protocol execution.Provide support in vendor management.Provide support between our CRO and Data Management vendor to ensure quality study data is collected and that study trends are closely tracked.Ensure that the overall study budget and study timeline targets are met. -
Clinical Research AssociateKelly Mar 2020 - Nov 2020Troy, Michigan, UsKelly OCG providing services for Johnson & Johnson Surgical VisionTreat my co-workers and clinical sites like extended members of my family.Monitor clinical trials, utilizing analytical risk-based monitoring, to ensure sponsor and investigator obligations are being met and are compliant with the study-specific Monitoring Plan, applicable local regulations, ICH/GCP guidelines, and IRB approvals.Ensure that Regulatory applications have been submitted and approvals received.Organize delivery of all study-specific materials to and from the clinical sites and ensure that the Investigator receives all study documents.Act as the first-line contact with clinical sites and report to the Trial Manager on all major siterelated issues. -
Clinical Research AssociateGlaukos Corporation Oct 2017 - Mar 2020Aliso Viejo, Ca, UsTreat study-site employees like members of my work family. Oversee implementation of study protocols and make certain quality data is collected at the site level. Ensure site’s PIs, Sub-Is, and Study Coordinators have a thorough understanding of the study protocol and feel comfortable implementing it in their practice. Offer guidance, based on GCP and ICH guidelines, on how to resolve study-related issues. Conduct site evaluation visits, site initiation visits, interim monitoring visits, site close-out visits. Assist in the creation of study source documents. -
Clinic DirectorVance Thompson Vision Apr 2016 - Aug 2017Sioux Falls, Sd, UsTreat my team like family and ensure our patients receive a customer experience second to none. Responsible for daily operations as administrator of a multi-specialty ophthalmology practice; including overhead management, expansion planning, taking customer service standards to a higher level, strategic planning, and choreographing marketing initiatives and practice development with our Sioux Falls office.Equal parts world-class reputation and medical start up. My team has the opportunity to bring the Vance Thompson Vision name to a new market. -
Clinical Research ManagerVance Thompson Vision Jun 2013 - Apr 2016Sioux Falls, Sd, UsI work to find clinical studies that fall in step with our company values and provide patients with a world-class experience and next generation technology. -
General ManagerThe Historic Town Hall Inn May 2011 - May 2013Oversee all day-to-day aspects of the hotel operations including guest relations, front desk, housekeeping, maintenance, finances, and establish priorities consistent with hotel objectives.Greet and register guests and arrange payment with guests.Maintain product and service quality standards through guest evaluations and operations.Ensures good safety practices of employees and guests, assisting in the maintenance of proper emergency and security procedures.Answer questions about hotel policies and resolve any guest issues.
Kelly Hall Skills
Kelly Hall Education Details
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Liberty UniversityGeneral -
Johns Hopkins University Advanced Academic ProgramsResearch Administration -
South Dakota State UniversityBiology
Frequently Asked Questions about Kelly Hall
What company does Kelly Hall work for?
Kelly Hall works for Orasis Pharmaceuticals
What is Kelly Hall's role at the current company?
Kelly Hall's current role is Associate Director Medical Affairs.
What is Kelly Hall's email address?
Kelly Hall's email address is ke****@****rma.com
What schools did Kelly Hall attend?
Kelly Hall attended Liberty University, Johns Hopkins University Advanced Academic Programs, South Dakota State University.
What skills is Kelly Hall known for?
Kelly Hall has skills like Clinical Research, Ophthalmology, Customer Service, Leadership, Teamwork, Clinical Trials, Public Speaking, Hotels, Hospitality, Hospitality Management, Project Management, Event Planning.
Who are Kelly Hall's colleagues?
Kelly Hall's colleagues are Beth Emerson, Linus Mason, Casey Richardson, Scott Rheault, Ilan Rubin, Jeff Francis, Luzi Andreas Von Bidder.
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