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10 часов назад

Clinical Research Coordinator II (Cancer Research)

47 924 - 59 894$
Формат работы
onsite/hybrid
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Clinical Research Coordinator II (Cancer Research) (Clinical Trials): Coordinating cancer clinical trials at Lowell General Hospital, including participant recruitment, informed consent, protocol-required visits, clinical procedures, and study data collection with an accent on regulatory compliance, participant safety, and data quality. Focus on screening eligibility, maintaining IRB and study documentation, resolving data queries, monitoring adverse events, and supporting sponsor site visits.

Location: Lowell General Hospital – Main Campus, 295 Varnum Ave, Lowell, MA 01854. On-site and hybrid work arrangements are stated.

Salary: $47,924.24–$59,894.75 per year.

Company

hirify.global provides clinical healthcare and supports clinical research studies through its medical institutions.

What you will do

  • Recruit and screen study participants, assess eligibility, explain studies, and obtain informed consent.
  • Coordinate protocol-required visits, follow-up activities, tests, procedures, and basic laboratory work.
  • Abstract source documents, complete case report forms and data entry, perform quality checks, and resolve data queries.
  • Maintain regulatory binders, study records, supplies, and participant information in accordance with confidentiality requirements.
  • Support Institutional Review Board requirements, adverse-event reporting, protocol compliance, and sponsor site visits.
  • Assist the Principal Investigator with planning and implementing assigned clinical research studies.

Requirements

  • Bachelor’s degree, or a high school diploma/equivalent with four years of related experience.
  • At least two years of experience in research-related activities.
  • Strong organization, attention to detail, data collection, record-keeping, prioritization, computer, communication, and interpersonal skills.
  • Ability to follow human-subject protection requirements, HIPAA regulations, FDA Good Clinical Practice guidelines, and institutional policies.
  • Ability to work at the Lowell General Hospital location under the stated on-site and hybrid arrangements.

Nice to have

  • Five years of research-related experience.
  • Previous clinical trial experience, preferably in cancer research.
  • IATA Hazardous Goods Shipping certification.
  • CITI Human Research Protection certification.
  • Basic Life Support certification, where required by the specific role.

Culture & Benefits

  • Full-time schedule of 40 hours per week, Monday through Friday.
  • Flexible schedule options of 7:00 a.m.–3:30 p.m. or 8:30 a.m.–5:00 p.m.
  • Four-day work week.
  • Comprehensive total rewards package supporting health, financial security, and career growth.

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