Top 14 Clinical research associate Jobs in Bethlehem Pa

Clinical Research Coordinator I (PA/NJ residents only)
St. Luke's University Health Network —Bethlehem, PA
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
Sr. Clinical Scientist/Associate Director, Clinical Science
Celldex Therapeutics, Inc. —Hampton, NJ
- $133,579 - $199,501 a year
- Full-time
- Microsoft Word
- 5 years
- Bachelor of Science
- Health savings account
- Paid holidays
Clinical Research Coordinator II- Advanced Research
Lehigh Valley Health Network —Allentown, PA
- Full-time
- Nursing
- Patient monitoring
- RN License
10d
Regulatory Coordinator I
St. Luke's University Health Network —Allentown, PA
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Administrative experience
Project Coordinator
Sharp Clinical Services —Bethlehem, PA
- Full-time
- Microsoft Word
- Mid-level
- Associate's degree
11d
Clinical Trials Assistant
Quakertown Veterinary Clinic —Quakertown, PA
- Part-time
- Computer literacy
- High school diploma or GED
- Data entry
Quick Apply
Senior Manager, Clinical Project Management
Olympus —Center Valley, PA
- $119,702 - $167,584 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Writing skills
- Paid parental leave
- Paid holidays
Pre Award Specialist
Lehigh Valley Health Network —Allentown, PA
- Full-time
- Nursing
- Microsoft Excel
- Microsoft Outlook
Director, Clinical Science, Cronos
IQVIA —Bethlehem, PA
- Full-time
- Remote
- Medicine
- Microsoft Outlook
- Management
- Work from home

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Clinical Research Coordinator I (PA/NJ residents only)

St. Luke's University Health Network -
Bethlehem, PA

Apply Now

Job Details

Full-time

Qualifications

Microsoft Excel
Microsoft Outlook
Medical terminology

Full Job Description

St. Luke's is proud of the skills, experience and compassion of its employees. The employees of St. Luke's are our most valuable asset! Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care.

The Clinical Research Coordinator (CRC) assumes a critical role in the research process. The CRC is responsible for the screening, enrollment, consenting, and coordination of clinical trials ensuring compliance with the protocol and all local, state, ICH/GCP Guidelines, and Federal regulations. The CRC is also responsible for maintaining quality data for all patients enrolled into clinical trials as assigned, ensuring timely and accurate data entry for trials as assigned.

JOB DUTIES AND RESPONSIBILITIES:

Demonstrates knowledge and practice of ICH/GCP guidelines, HIPPA Regulations and Confidentiality Policies related to clinical research
Sound conduct of the clinical trial, including but not limited to, recruitment, screening, enrollment, and follow-up of eligible subjects according to protocol requirements. This includes performing required study procedures as applicable. Apply knowledge and skills to independently review new protocols, consents, and other clinical trials documents to ensure protocol compliance
Review and extract data from medical charts to screen patients for eligibility for assigned protocols
Review consent form, protocol procedures, and treatment regimen with potential patients and obtain consent from interested participants, documenting the consent process as required
Maintenance of accurate and complete documentation, including but not limited to regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, subjects logs and study-related communication.
Organizational management of all aspects of the trial including but not limited to timeliness in completing case report forms (CRFs), data entry, reporting adverse drug events, managing caseload and managing study files.
Obtain data from other departments (radiology, pathology, etc.) as required by each protocol.
Prepare research charts for monitoring visits and audits.
Respond to data queries and collate data as requested by research group or investigator, and maintain quality source documentation.
Review charts for adverse events and submit appropriate documentation
Submit follow-up information as specified by protocol. Long-term survival follow-up may require extensive time acquiring medical records from other physician offices, patient and/or family contact, or correspondence with regulatory agencies.
Supports conduct of clinical trials, including travel to physician offices and national meetings/conferences
Communication of all protocol-related issues/problems, and other relevant study information to the appropriate medical and management staff.
Professional conduct in the presence of subjects, research staff, sponsors, monitors, etc.
Provide direction/training to other members of research staff as appropriate. For example, guidance to clinical research associate in completing case report forms.
Preparation and shipping of laboratory specimens to study (central) laboratories and maintenance of appropriate certifications related to this function (for example, IATA training).

PHYSICAL AND SENSORY REQUIREMENTS:

Requires sitting for up to seven hours per day, 3 hours at a time. Standing for up to 4 hours per day, 3 hours at time. Requires occasional fingering, handling and twisting and turning. Occasionally requires lifting, carrying and pushing and pulling objects weighing up to 25 pounds. Occasionally requires reaching above shoulder level. Must have the ability to hear as it relates to normal conversation, seeing as it relates to general vision.

EDUCATION:

Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred. Must be familiar with medical terminology.

TRAINING AND EXPERIENCE:

Required knowledge of Microsoft Office Programs: Word, Excel, Access, Outlook; Internet Functions. Experience in health-related field (2 years) required. One year experience in clinical research highly preferred.

Please complete your application using your full legal name and current home address. Be sure to include employment history for the past seven (7) years, including your present employer. Additionally, you are encouraged to upload a current resume, including all work history, education, and/or certifications and licenses, if applicable. It is highly recommended that you create a profile at the conclusion of submitting your first application. Thank you for your interest in St. Luke's!!

St. Luke's University Health Network is an Equal Opportunity Employer.

Apply Now

Refine Your Search

clinical research associate jobs in bethlehem pa

Clinical Research Coordinator I (PA/NJ residents only)

Sr. Clinical Scientist/Associate Director, Clinical Science

Clinical Research Coordinator II- Advanced Research

Regulatory Coordinator I

Project Coordinator

Clinical Trials Assistant

Senior Manager, Clinical Project Management

Pre Award Specialist

Director, Clinical Science, Cronos

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St. Luke's University Health Network is an Equal Opportunity Employer.

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