Hi, my name is Wesley. I currently work as an Environmental Health and Safety Specialist for Actalent at Project Kuiper. My experiences include an Associates in Musical Theory, work in stage production, and 16 years as a Volunteer Firefighter/EMT. I am hoping to find remote voice acting/voice over work for supplemental income and to develop new skills.More...
Imani Mapp
HR Assistant Administrator@Actalent
Verified
Elancheliyan Ravichandran, CID
Associate Project Manager@Actalent
Verified
I have worked on many successful projects as an Associate Project Manager at Actalent. I have played a key role in the successful completion of these projects by managing and coordinating the work of the project team, as well as providing support to the project manager. I have also been responsible for the development and implementation of project plans, as well as the monitoring and reporting of project progress. In addition, I have also provided training and mentorship to new project team members.More...
Nadine Aladarah
Talent Acquisition/Recruitment lead@Actalent
Verified
10 years of agency recruitment with two years being in talent acquisitionMore...
Alex Miller
Talent Acquisition Specialist
Verified
I am a 10 year biotech recruitment professional focusing from early phase development through commercial operations. Positions placeded range from entry level to C-SuiteMore...
Donna Symanietz
Clinical Research Professional
Verified
Summary:
• 20 plus years experience in the pharmaceutical, medical device, and CRO industries
• 10 years in National Management and Training
• Knowledgeable in clinical trial operations from feasibility through to closeout.
• Experience in FDA regulations 21 CFR, Parts 11,50,54, and 56
• Skillful in maintaining the regulatory binder, which houses essential documents such as1572, source
documents, DOA, training Logs, ICF, SAE forms, Financial Disclosures, Subject Enrollment &
Identification Logs, Case Report Forms (CRF), Procedure manuals, Standard Operating Procedures
(SOP), Site Visit Logs, Correspondences, Trial Master Files (TMF) and other Investigator Site File (ISF)
document.
• 2 years Phase 4 research projects
• Pharmacovigilance Leadership
• Clinical Research Site Activation Coordinator
Specialties:
Sales, Account Management and Project Management. Extensive medical knowledge and experience with multiple therapeutic areas. Proven track record in both the large and small pharma environments and extensive experience with CRO’s. Expert with contract negotiations with health systems at CFO and CEO level.Summary: • 20 plus years’ experience in pharmaceutical, medical device, and CRO industries • 10 years in National Management and Training • Knowledgeable in clinical trial operations from feasibility through to closeout. • Experience in FDA regulations 21 CFR, Parts 11,50,54, and 56 • Skillful in maintaining the regulatory binder, which houses essential documents such as1572, source documents, DOA, training Logs, ICF, SAE forms, Financial Disclosures, Subject Enrollment & Identification Logs, Case Report Forms (CRF), Procedure manuals, Standard Operating Procedures (SOP), Site Visit Logs, Correspondences, Trial Master Files (TMF) and other Investigator Site File (ISF) document. • 2 years Phase 4 research projects • Pharmacovigilance Leadership • Clinical Research Site Activation Coordinator Specialties: Sales, Account Management and Project Management. Extensive medical knowledge and experience in More...
Rachael Chen
HR Recruiter/Generalist@Samsung Electronics America