Clinical Trial Associate

Why Pharm-Olam:Pharm-Olam, LLC is a mid-size Contract Research Organization (CRO) that has a massive global reach.We are a company that strives to deliver cost-effective, quick-to-market clinical services in today's emerging marketplace.Pharm-Olam has one of the largest global footprints of any CRO today and we are committed to not only maintain our standard, but to continue to strengthen our presence even further.We offer a unique working environment with a global team culture, competitive salary and benefits package.This is Important Work:Acts as the primary administrative support to Pharm-Olam clinical study teams, as required by Project Managers and Sponsors, thus ensuring that the clinical trial is conducted in accordance with international regulatory and local regulatory and ethical laws, and guidelines for Good Clinical Practice and Standard Operating Procedures.Assists the study team with the day-to-day conduct of international clinical studies with the guidance of an experienced team member.Your Role:- Assists CRAs, Lead CRAs (LCRA), Clinical Team Leaders (CTL) and Project Managers (PM) with the day-to-day administration of clinical studies.- Tracks critical documents and informs PM / CTL and/or LCRA of outstanding documents.- Accurately updates and maintains clinical systems within project timelines.- Prepares, distributes, files, and archives clinical documentation.- Reviews study files periodically for accuracy and completeness.- Prepares and distributes clinical trial supplies and maintains tracking information.- Assists PM / CTL / LCRA / CRAs with collection and filing of critical documents.- Attends local Investigator and CRA meetings.Records questions and answers, and coordinates with the hotel staff to ensure smooth running of the meeting.- May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.- Performs administrative tasks to support team members with clinical trial execution, as required.- Prepares Trial Master File according to Pharm-Olam SOPs with the guidance of Project Manager and/or experienced CTAs, as required.- Assists with the preparation of Investigator Site Files, Investigator Manuals and Training Manuals with the guidance of Project Manager, experienced CTAs, as required.- Assists with returning/archiving study files.- As needed, communicates with sites regarding trial start-up, conduct, and close-out activities at requested intervals.- May participate in feasibility and/or site identification activities.- May attend clinical teleconferences, and prepares and distributes minutes for Sponsor and Project Teams within agreed timelines.**Your Team**:- Reports to Clinical Trial Associate Manager, COM or designee.- Collaborates with project teams and all Pharm-Olam staff.Required Education and Qualifications:- Fluency in English (spoken and written)- Customer service orientation- Strong verbal and written communication skills- Computer literacy, proficiency in Microsoft Office- Excellent interpersonal and organizational skills- Ability to work independently and to effectively prioritize tasks- Ability to manage multiple projects- Attention to detail- Ability to establish and maintain effective working relationships with co-workers and managers.Pharm-Olam, LLC provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.To connect with our community, follow Pharm-Olam on LinkedIn.