CLINICAL TRIALS STUDY COORDINATOR

ADP, Inc.; Fort Gratiot Charter Township (MI); Presencial; USD 52 000 - 76 000; Tempo integral

Resumo da oferta

ADP, Inc. in Michigan is seeking a Full Time Clinical Trials Study Coordinator for Canton and Ann Arbor. This on-site role is Mon–Thu with travel between locations; Mon and Tue will be in Ann Arbor, Wed and Thu in Canton.

The CRC will manage trial conduct under the PI, collect health data, ensure GCP compliance, and coordinate with Investigators, CROs and Sponsors to support study activities. Ideal candidates have at least 2 years of CRC experience and CCRP/CCRC certification preferred, with

Qualificações

• CCRC/CCRP certification preferred.
• 2+ years of CRC or clinical research experience.

Responsabilidades

• Coordinate trials under PI per FDA, GCP and protocol.
• Collect subject health data and assess eligibility.
• Maintain source documents, EDC and CTMS data entry.
• Coordinate with CROs, sponsors and site staff.

Conhecimentos

CCRC/CCRP

Communication

Organizational skills

Interpersonal skills

Descrição da oferta de emprego

We are seeking a Full Time, Mon-Thurs, on-site Clinical Trials Study Coordinator for our Canton and Ann Arbor locations. Must be willing to travel to both locations. Mon and Tues will be at our Ann Arbor location, Wed and Thurs at our Canton location.

Summary:

The Clinical Research Coordinator is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the vision and mission of the company. The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned trials. The CRC follows study specific protocol guideline and communicates and interacts with Investigators, clinic staff, CROs and Sponsors to effectively perform clinical research and coordinate research activities. All duties carried out by the CRC are done so in accordance with company policies, SOPs, and Good Clinical Practice (GCP) as well as all applicable local, state and federal regulations.

Primary Responsibilities:

• Coordinate clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines.
• Identify potential problems or inconsistencies and take action as appropriate.
• May be asked to draw blood occasionally.
• Articulate protocol issues to CRO and/or Sponsor, Site Lead, Manager, Principal or Sub-Investigator, and other members of the study team.
• Collect initial subject health and demographic information by interviewing subjects and accessing other appropriate sources.
• Review subject comprehensive medical documentation to determine protocol eligibility under the supervision of the Principal Investigator.
• Ensure a flow of communication including telephone conferences between subject, study staff, referral sources and recruitment team, Sponsor and/or CRO, Monitor(s) and Auditors, if applicable.
• Perform clinical tasks including, but not limited to: vital signs, height and weight, ECG, phlebotomy, specimen processing and packaging.
• Maintain timely internal source documentation as well as sponsor-required information.
• Maintain timely EDC data entry and query resolution.
• Maintain timely CTMS data entry of patient visits and study information.
• Complete Verification of subjects before consenting.
• Report hospital census data, if applicable.
• Dispense and maintain accurate records of investigational and study product.
• Educate subject and family members regarding specific studies and clinical drug trials in general.
• Complete all monitor and sponsor queries in a timely manner.
• Perform Quality Control (QC) checks on all trials per company SOP and interface with QA Director as needed.

Recruitment Responsibilities:

• Send “All Users” email upon enrollment activation or enrollment closure
• Participate in recruitment planning meetings prior to study start
• Provide weekly updates to Active Studies Report
• Communicate all advertising needs to recruitment team
• Maintain weekly communication with recruitment team in order to maximize recruitment in all enrolling trials
• Communicate the need for study or company flyers

Secondary Responsibilities:

Maintains Quality Service and Departmental Standards by

• Reading, understanding and adhering to organizational Standard Operating Procedures (“SOP”)
• Assisting in establishing and enforcing departmental standards

Contributes to team effort by

• Working with internal staff to resolve issues
• Exploring new opportunities to add value to the organization and departmental processes
• Helping others at the site to achieve site goals
• Performing other duties as assigned
• Support the organization’s mission and goals

Maintains Technical and Industry Knowledge by

• Attending and participating in applicable company-sponsored training
• Attending and participating in Sponsor investigator meetings, recruitment meetings, and trainings

Skills And Qualifications:

CCRC or CCRP certification preferred

• Strong motivational skills and abilities – promoting a team-based approach
• Strong interpersonal and communication skills, both verbal and written
• Strong organizational and leadership skills
• Goal oriented
• Ability to maintain a professional and positive attitude
• Strong critical thinking skills
• Strong ability to multi-task
• Ability to support and demonstrate the mission and goals of the company
• Excellent interpersonal and customer service skills
• Knowledge of medical terminology and clinical practices

Experience:

At least 2 years of experience as a CRC in clinical research or relevant clinical role

Nothing in this position description restricts management’s rights to assign or reassign duties and responsibilities to this position at any time.