(Hybrid) Oncology Clinical Research Specialist - WVU Cancer Institute/Clinical Research Unit

West Virginia University Research Corporation; Morgantown (WV); Hybrid; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a dedicated Oncology Clinical Research Specialist to join their innovative team. This pivotal role involves managing clinical trials, ensuring compliance with protocols, and enhancing patient recruitment strategies. You'll play a crucial part in the research process, working collaboratively with a talented team to drive impactful results. This position offers a hybrid work environment, promoting a healthy work-life balance while contributing to groundbreaking research in oncology. If you're passionate about clinical research and patient care, this opportunity is perfect for you.

Benefits

13 Paid Holidays

Paid Time Off (PTO)

403(b) Retirement Savings

Health Insurance Options

Dependent Education Scholarship

WVU Perk

Qualifications

• Bachelor's degree in allied health or related field is required.
• Minimum of two years experience in clinical setting or research.

Responsibilities

• Manage and coordinate clinical trials ensuring protocol compliance.
• Lead patient recruitment and documentation efforts for trials.

Skills

Clinical Trials Research

Patient Care

Data Collection and Analysis

Communication Skills

Problem-Solving

Education

Bachelor's Degree in Allied Health or Related Field

Job description

Description

West Virginia University Research Corporation is currently accepting applications for a (Hybrid) Oncology Clinical Research Specialist with the WVU Cancer Institute/Clinical Research Unit

About the Opportunity

Participates in the development, coordination, and implementation of research and administrative strategies essential to the successful management of clinical trials research conducted by WVU Cancer Institute faculty at West Virginia University Cancer Institute. Performs a variety of independent and collaborative duties involved in Phase I - IV clinical trial coordination and implementation, organization, oversight, documentation, tracking, data abstraction and collection and compilation of clinical research data. This position may also assist on other studies, as needed.

This position serves as a resource contact relative to the WVU Cancer Institute Clinical Research Unit. Independently uses professional concepts and techniques, as well as organizational policies to solve a wide range of moderate to complex problems in imaginative and practical ways. Depth, skills, knowledge, and interpretive abilities, as well as some creativity, are required to successfully perform duties. Work effort often addresses non-routine matters within established protocol, guidelines, and/or policies. Work effort has significant impact on client services and operations, producing moderate to major organizational, legal and financial results and/or liabilities. Position duties may require oversight of projects or programs, including coordination of work by others providing support of basic objectives.

At WVU Research Corporation, we strongly believe in work-life balance and keeping time for things we love outside our work. WVU Research Corporation offers a comprehensive benefits package with a variety of options to suit your needs:

• 13 paid holidays (staff holiday calendar)


• Paid Time off (PTO)


• 403(b) retirement savings with a fully vested 3% employee contribution match, (Employees have the option of contributing an additional 1-3% of their earnings to the plan, which is also matched by the WVURC)


• A range of health insurance and various other benefits


• Dependent Education Scholarship


• WVU Perk

What You'll Do

• Protocol Compliance: Facilitates compliance with the requirements of the research protocol and good clinical research practice while remaining cognizant of the needs of diverse patient populations.


• Clinical Trials-Related Communication: Utilizes multiple communication methods to facilitate the effective conduct of clinical trials.


• Informed Consent Process: Demonstrates leadership in ensuring patient comprehension and safety during initial and ongoing clinical trial informed consent discussions.


• Management of Clinical Trial Patients: Involves a variety of resources and strategies to manage the care of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and reporting requirements as well as management of symptoms.


• Documentation: Provides leadership to the research team in ensuring collection of source data and completion of documentation that validate the integrity of the conduct of the clinical trial.


• Patient Recruitment: Utilizes a variety of strategies to enhance recruitment while being mindful of the needs of diverse patient populations.


• Ethical Issues: Demonstrates leadership in ensuring adherence to ethical practices during the conduct of clinical trials in order to protect the rights and well-being of patients and the collection of quality data.


• Financial Implications: Identifies the financial variables that affect research and supports good financial stewardship in clinical trials.


• Professional Development: Takes responsibility for identifying his or her ongoing professional development needs and seeks resources and opportunities to meet those needs, such as through membership in nursing, disease specialized (i.e. oncology nursing society), or research organizations.

Qualifications

• Bachelor's degree from an allied health discipline, or related medical field (such as nursing, medical technology, pharmacy, etc.)


• A minimum of two (2) years of experience in the following:
  
  
  
  • Working in a clinical setting and/or experience in clinical research.
  
  
  
  


• Any equivalent combination of related education and/or experience will be considered.


• All qualifications must be met by the time of employment.
  

Knowledge, Skills and Abilities

• Knowledge of clinical trials research.


• Must possess and apply knowledge of many different and unrelated processes and methods related to such areas as:
  
  
  
  • Patient care - information and techniques needed to diagnose and treat human injuries, diseases, and deformities. This includes symptoms, treatment alternatives, drug properties and interactions, and preventive health-care measures.
  
  
  • Treatment design, administration and modification.
  
  
  • Counseling and education - principles and methods for training design, teaching and instruction for individuals and groups, and the measurement of training effects.
  
  
  • Data collection, validation, entry, analysis, and reporting.
  
  
  • Human subjects protection and related issues - knowledge of professional principles (GCP and IRB guidelines), legal and/or reporting requirements affecting grants and contracts, and adheres to industry and government standards.
  
  
  
  


• Skilled at being aware of others' reactions and understanding why they react as they do.


• Skilled at communicating effectively in writing as appropriate for the needs of the audience.


• Skilled at using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approached to problems.


• Knowledge of principles and processes for providing customer and personal services. This includes customer needs assessment, meeting quality standards for services, and evaluation of customer satisfaction.


• Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. Position requires excellent customer service skills and the ability to communicate effectively with patients and families; pharmaceutical company personnel; regulatory and monitoring agency personnel; and, internal staff members. Communicates with physicians, patients, students and employees of WVU, WVU Hospitals, MBRCC and UHA.


• Ability to develop constructive and cooperative working relationships with others and maintain them over time.


• Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures or governmental regulations.


• Ability to write reports, business correspondence, and procedure manuals.


• Ability to arrange things or actions in a certain order or pattern according to a specific rule or set of rules (e.g., patterns of numbers, letters, words, pictures, mathematical operations).


• Ability to combine pieces of information to form general rules or conclusions (includes finding a relationship among seemingly unrelated events).


• Ability to analyze information and evaluate results to choose the best solution, solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.


• Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule form.


• Ability to develop specific goals and plans, to prioritize, organize and accomplish tasks independently and through others.

Requirements

• Within three (3) years of employment, incumbent must obtain certification as a Research Coordinator through the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA) is required.


• If applicable, valid RN license from the State of West Virginia.

About Research Corporation

The WVURC was created as a not-for-profit corporation in 1985 to support research (R1) at West Virginia University. We provide evaluation, development, patenting, management, and marketing services for inventions of the faculty, staff and students of the University.

The WVURC receives and administers funds awarded by external agencies for research and other activities and is responsible for helping protect intellectual property through patents, copyrights and licensing agreements for start-up companies based on University research.

West Virginia University Research Corporation is an Equal Opportunity Employer. We invite all qualified applicants regardless of race, color, religion, sex, national origin, age, disability, genetic information, or Veteran status.

Job Posting:Mar 18, 2025

Posting Classification:Research Corporation

Exemption Status:Exempt

Benefits Eligible:Yes

Schedule:Full-time