1 день назад
GoClinical Project Coordinator (GoClinical)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
GoClinical Project Coordinator (GoClinical/CTMS): Coordinating clinical study data, site communications, decentralized visits, document workflows, inventory, and logistics across clinical research programs with an accent on study setup, source document management, and sponsor and site coordination. Focus on tracking study metrics, auditing CTMS and GoClinical records, coordinating sample delivery, and supporting study closeout and equipment reconciliation.
Location: United States; remote work is supported, with hybrid work encouraged for new hires within a reasonably short commute of an office, as agreed with the manager.
Company
provides consulting solutions across regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology for biotech, medical device, and pharmaceutical organizations.
What you will do
- Create, maintain, and update study, sponsor, site, contact, subject, visit, and issue details in CTMS and GoClinical.
- Coordinate day-to-day communications with clinical sites, sponsors, CROs, central laboratories, and vendors.
- Manage site setup, including decentralized visit introductions and training.
- Receive, track, review, manage, and distribute source documents from decentralized visits.
- Coordinate visit scheduling, courier bookings, sample collection and delivery, inventory, and shipment tracking.
- Track study metrics, support audits and closeout activities, and reconcile returned field equipment and study systems.
Requirements
- At least 2 years of experience in clinical studies or research, healthcare, or a related field.
- Bachelor’s degree or equivalent experience, with at least 3 years of combined relevant education, knowledge, and skills.
- Current knowledge of and ability to apply ICH/GCP requirements, applicable regulations, guidelines, SOPs, and global regulations.
- Strong organization, multitasking, communication, initiative, and independent and collaborative working skills.
- Advanced computer skills; experience with Microsoft Word, Excel, PowerPoint, and Adobe Acrobat is preferred.
Culture & Benefits
- Remote work is supported, with in-person collaboration encouraged where practical.
- Inclusive workplace focused on diversity, equity, and inclusion.
- Employees are encouraged to work collaboratively, innovatively, and entrepreneurially.
- Applications are personally reviewed by the recruitment team without AI screening tools.
- Applicants receive an outcome regarding their application.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →
Похожие вакансии
2 дня назад
Project Specialist (Clinical Research)
2 дня назад
Project Manager - Clinical Trial Operations Exp. Req. (Job 1421)
90 000 - 110 000$
6 дней назад
Project Coordinator (Clinical Operations)
54 - 69$
13 часов назад
Clinical Research Engagement Lead (Pharma)
103 300 - 191 900$
2 дня назад
Project Assistant, Healthcare Transformations
26 - 32$
1 день назад
TIME Operations Manager
65 000 - 110 000$