Clinical Research Coordinator III

DM Clinical Research; Philadelphia (Philadelphia County); Presencial; USD 60.000 - 90.000; Jornada completa

Descripción de la vacante

A clinical research organization in Philadelphia seeks a Clinical Research Coordinator III to ensure quality research at investigative sites. The ideal candidate will have over 5 years of clinical research experience and be well-versed in FDA regulations and ICH/GCP guidelines. Responsibilities include overseeing study visits, adhering to documentation standards, and maintaining knowledge of protocols. This role requires strong communication skills and the ability to mentor staff, ensuring study enrollment goals are met efficiently.

Formación

• Minimum of 5 years experience in Clinical Research.
• Experience in supervising preferred.
• Wide therapeutic range of clinical trials experience preferred.
• Regulatory research experience is a plus.

Responsabilidades

• Conducting and overseeing study subject visits and documenting.
• Adherence to ALCOA-C Standards with clinical trial documentation.
• Maintaining a working knowledge of FDA regulations and ICH-GCP guidelines.
• Complete data entry and resolve queries per internal guidelines and sponsor expectations.
• Train and mentor site staff as needed and supervise visit preparedness for sponsor/CRO visits.
• Coordinate with Laboratory, Data, Administrative, Investigators, and Sponsor teams.
• Maintain knowledge of FDA regulations, ICH-GCP, SOPs and study protocols.
• Monitor recruitment and retention for assigned protocols at sites.

Conocimientos

Detail-oriented

Proactive

Strong written communication

Excellent customer service skills

Regulatory knowledge

Educación

High School Diploma or equivalent

Bachelor's degree

Foreign Medical Graduates

Herramientas

ACRP certification

Descripción del empleo

Position: Clinical Research Coordinator III

Location: Philadelphia, PA

Job Id: 1108

# of Openings: 1

Clinical Research Coordinator III

The Clinical Research Coordinator III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations and to ensure company goals are achieved on a timely basis.

DUTIES & RESPONSIBILITIES

• Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
• Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
  • Sponsor-provided and IRB-approved Protocol Training
  • All relevant Protocol Amendments Training
  • Any study-specific Manuals Training, as applicable
  • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
• Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
• Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
• Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
• Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
• Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
• Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
• Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
• Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
• Ability to train and mentor site staff, as needed
• Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
• Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
• Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
• Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
• Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
• Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
• Being prepared for and available at all required company meetings.
• Submitting required administrative paperwork per company timelines.
• Occasionally attending out-of-town Investigator Meetings
• Any other matters as assigned by management

KNOWLEDGE & EXPERIENCE

Education:

• High School Diploma or equivalent required
• Bachelor's degree preferred
• Foreign Medical Graduates preferred

Experience:

• Minimum of 5 years experience in Clinical Research
• Supervisory experience preferred
• Wide therapeutic range of clinical trials experience preferred
• Regulatory research experience is a plus

Credentials:

• ACRP or equivalent certification is preferred

Knowledge and Skills:

• Goals-driven while continuously maintaining quality.
• Must be detailed-oriented, proactive, and able to take initiative.
• Must have strong written and communication skills.
• Must have excellent customer service skills.