top of page
shutterstock_1060198448.jpg

Looking for a new role?

You may view our publicly advertised roles and apply here

As a Principal Investigator for Neurology Trials within the Wellnext network, you will play a pivotal role in planning, executing, and overseeing clinical trials while collaborating with our organization to enhance neurology research. Your expertise and leadership will guide our research efforts, ensuring the highest quality of patient care, safety, and scientific rigor.

Responsibilities
 

  • Clinical Trial Leadership:

    • Lead the development and execution of neurology clinical trials within our network, from study design to final data analysis and reporting

    • Ensure compliance with regulatory requirements, ICH-GCP guidelines, and ethical standards in all trial activities

    • Collaborate with cross-functional teams, including medical, regulatory, and clinical operations, to ensure the successful conduct of trials

  • Patient Care:

    • Provide medical oversight for patients participating in clinical trials, ensuring their well-being and safety

    • Engage with patients and their families, addressing their concerns, and explaining the trial processes and potential benefits

  • Study Design and Protocol Development:

    • Contribute to the design of neurology trials, including the development of study protocols, informed consent forms, and case report forms

    • Participate in the identification of relevant endpoints and the selection of appropriate study populations

  • Data Analysis and Reporting:

    • Oversee data collection, analysis, and interpretation of trial results

    • Prepare high-quality scientific reports and publications for regulatory submissions and conferences

  • Collaboration and Networking:

    • Foster collaborations with key opinion leaders, investigators, and external partners in the field of neurology

    • Represent Wellnext at scientific conferences, seminars, and meetings

  • Regulatory Affairs:

    • Work closely with our regulatory affairs teams to ensure compliance with all regulatory submissions and approvals

    • Assist in preparing and reviewing regulatory documents, such as INDs and NDAs

​

Requirements
 

  • Medical Doctor (MD)

  • Board certification in neurology.

  • Experience as a Principal Investigator in neurology clinical trials will be preferred but not necessary

  • Strong understanding of clinical trial design, protocol development, and regulatory requirements

  • Exceptional communication and interpersonal skills for patient care and collaboration

  • Proficiency in data analysis and interpretation

  • Knowledge of Good Clinical Practice (GCP) guidelines and ethical principles

  • Ability to work in a multidisciplinary team and lead by example

  • Strong commitment to patient welfare and advancing neurologic treatment Benefits

  • Attractive compensation and benefits package

  • Opportunities for professional development and continuing medical education

  • Access to Wellnext's network of leading neurology experts

  • The chance to make a meaningful impact on neurology research and patient care

  • Collaborative and dynamic work environment

  • Joining a network of experienced professionals in neurology research
     

If you are a dedicated and experienced neurologist passionate about advancing neurologic treatment through clinical trials, we encourage you to apply as a Principal Investigator for Neurology Trials. 

Our client Wellnext is seeking a dedicated Clinical Research Coordinator (CRC) to join our team in Washington, Missouri, for an industry-funded clinical trial focusing on Severe Community Acquired Pneumonia (CAP) in the Respiratory/Critical Care field. The CRC will play a crucial role in the successful execution of this project.

Responsibilities

​

  • Patient Recruitment and Screening:
    Identify and screen potential participants for the clinical trial.
    Ensure that all recruited participants meet the eligibility criteria.

 

  • Informed Consent:
    Explain the trial details to participants and obtain informed consent.

 

  • Data Collection and Management:
    Collect, record, and maintain accurate and complete study data.

 

  • Patient Monitoring:
    Utilize expertise in incubating patients as required by the study protocol.

 

  • Compliance and Quality Assurance:
    Monitor and ensure adherence to study protocols and ethical standards.

 

  • Communication:
    Maintain clear and effective communication with study investigators, participants, and
    healthcare staff.

 

  • Documentation:
    Maintain comprehensive study documentation and regulatory compliance.

 

  • Project-Based Work:
    This position is project-based, and the salary will be determined once the project is approved and begins.

 

​

Requirements

 

  • Bachelor's degree in a relevant field (Nursing, Life Sciences, or others).

  • Certified Clinical Research Coordinator (CCRC) credential from the Association of Clinical Research Professionals (ACRP).

  • Experience in clinical research, with a focus on Respiratory/Critical Care trials.

  • Proficiency in intubating patients is a must.

  • Strong attention to detail and organizational skills.

  • Excellent communication and interpersonal abilities.

  • Knowledge of Good Clinical Practice (GCP) guidelines.

  • Willingness to work on a project-based, as-needed basis.

​

form
bottom of page