Vacancy caducado!
PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose - to improve health.PPD’s Clinical Management department is committed to industry leadership and the relentless pursuit of excellence. Working in the Clinical Management department, you will combine deep knowledge, therapeutic expertise, and robust tools to help our clients deliver life-changing therapies to market.Responsibilities include, but are not limited to;Perform the receipt and filing of hardcopy and electronic documents related to clinical studies and programs.
Process hard copy documents, review documents and file in appropriate folder structures. Process and lock scanned documents, review documents and file in appropriate folders.
Create new files as appropriate.
Fulfill record retrieval, photocopy and scan requests.
Provide appropriate and timely updates to users about document status.
Perform QC of documents to ensure the accuracy of hardcopy and electronic filing.
Participate in initiatives to establish or improve document management standards and processes.
Assist on special projects within area and train others in routine or specific tasks as needed; may provide direction to Clinical Document Assistant.
At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It's not just talk - our award winning training programs speak for themselves.To learn how PPD can advance your career, apply now!What To Expect NextWe look forward to receiving your application. A member of our talent acquisition team will review your qualifications and if interested, you will be contacted for an interview.QualificationsEducation and Experience:Associate's Degree or equivalent required
Knowledge, Skills and Abilities:Associate’s Degree or equivalent required
Two to 4 years experience in records management or information services, preferably in the pharmaceutical industry.
Must have intermediate proficiency in document processing and archiving software and hardware systems. Demonstrated experience in working with electronic document management systems required.
General understanding of the clinical research and development process and experience handling associated documents preferred.
Strong problem solving and organizational skills and attention to detail.
Effective interpersonal skills.
/PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:/Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner
Able to work upright and stationary for typical working hours
Ability to use and learn standard office equipment and technology with proficiency
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities
May require travel (Recruiter will provide more details)
Job: Clinical AdministrationOrganization: US BUTitle: Client-Dedicated - Sr Clinical Trial Coordinator / Document Specialist - Home BasedLocation: IL-North ChicagoRequisition ID: 179413PPD is an affirmative action employer that values diversity as a strength fosters and environment of mutual respect. PPD provides equal employment opportunities without regard to age, race, color, pregnancy, national origin, religion, sex, gender identity, sexual orientation, disability, veteran status or other status within any other protected group
Vacancy caducado!