Clinical Research Coordinator Position Available In Philadelphia, Pennsylvania

Philadelphia, PA
3 DAYS AGO
21521443
Summary
Philadelphia, PA
Competitive Salary
2 Years Experience
High school graduate or equivalency certificate (GED)
No Commisssion
40.00 hours per week / Day Shift /Full-Time
Description Reference #: 1017035

SHIFT:

Day (United States of America) Seeking Breakthrough Makers Children’s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation. At CHOP, your experience is valued; your voice is heard; and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care-and your career. CHOP’s Commitment to Diversity, Equity, and Inclusion
CHOP is committed to building an inclusive culture where employees feel a sense of belonging, connection, and community within their workplace. We are a team dedicated to fostering an environment that allows for all to be their authentic selves. We are focused on attracting, cultivating, and retaining talent who can help us deliver on our mission to be a world leader in the advancement of healthcare for children. We strongly encourage candidates of all races, colors, ethnicities, religions, perspectives, sexes, backgrounds, and lived experiences to apply. A Brief Overview
Under moderate supervision from study PI or other research study management staff, this role provides substantial coordination level support for all clinical research activities within the scope of clinical research protocols.
Seeking a clinical research coordinator (CRC) to support a translational research Bacterial Genome Sequencing project examining bacterial populations in infants and the NICU environment. The CRC will be expected to accomplish:
Regulatory tasks: maintaining and updating IRB protocol including IRB amendments, continuing reviews, updates to consent forms etc.
Patient recruitment/obtaining consent for obtaining skin, nasal, stool samples etc.
Performance of environmental sampling
Sample collection and sample organization (labeling samples, maintaining sample log, coordinating sample transfer with IDDL and microbiome center,etc),
May need to support technical tasks around sample processing and storage (should be willing to learn/help with centrifuging, plating etc if needed).
Data management of clinical, laboratory and microbiome data, simple data analytic tasks

• should be comfortable with Excel, Redcap, etc,
  Communicating, supporting and coordinating targeted infection prevention interventions with NICU nursing and environmental staff What you will do
  Core responsibilities
  Adhere to an IRB approved protocol
  Participate in the informed consent process of study subjects
  Support the safety of clinical research patients/research participants
  Coordinate protocol related research procedures, study visits, and follow-up care
  Screen, recruit and enroll patients/research participants
  Maintain study source documents
  Under the supervision of PI Report adverse events
  Understand good clinical practice (GCP) and regulatory compliance
  Educate subjects and family on protocol, study intervention, etc.

Comply with Institutional policies, standard operating procedures (SOPs) and guidelines, and with HIPAA and management of confidential materials
Must comply with federal, state, and sponsor policies
For multi-site studies or collaborations, support communication and meeting scheduling across teams
Related responsibilities
Manage essential regulatory documents
Register study on ClinicalTrials.gov as appropriate
Complete case report forms (paper & electronic data capture) and address queries
Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie,DSMB, independent safety officer)
Facilitate pre-study, site qualification, study initiation, and monitoring visit as appropriate
Facilitate study close out activities as appropriate
Coordinate research/project team meetings
Collect, process and ship samples as applicable to the protocol
Schedule subject visits and procedures
Retain records/archive documents after study close out Education Qualifications
High School Diploma / GED

• Required
  Bachelor’s Degree
• Preferred Experience Qualifications
  At least two (2) years of clinical or research related experience
• Required
  At least three (3) years of clinical or research related experience
• Preferred Skills and Abilities
  Basic knowledge of IRB and human subject protection
  Strong verbal and written communications skills
  Strong time management skills
  Ability to collaborate with stakeholders at all levels To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community.

As a condition of employment, professionals working onsite-at any CHOP location, for any portion of time-must be vaccinated for

COVID-19.

Learn more.

EEO / VEVRAA

Federal Contractor | Tobacco Statement

SALARY RANGE

$51,730.00

• $64,660.00 Annually Salary ranges are shown for full-time jobs. If you’re working part-time, your pay will be adjusted accordingly.
• At CHOP, we are committed to fair and transparent pay practices.

Factors such as skills and experience could result in an offer above the salary range noted in this job posting. Click here for more information regarding CHOP’s Compensation and Benefits. Children’s Hospital of Philadelphia is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability or protected veteran status.