Sub Investigator

Sub Investigator

Chester-le-Street Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead clinical trials, mentor staff, and ensure patient safety while collecting accurate data.
  • Company: Velocity Clinical Research is dedicated to innovative medical treatments and high-quality patient care.
  • Benefits: Enjoy medical, dental, vision insurance, paid time off, 401(k) match, and an annual incentive programme.
  • Why this job: Join a mission-driven team that values your contributions and supports career growth in clinical research.
  • Qualifications: Must be a licensed MD, DO, NP, or PA with 5+ years of clinical management experience.
  • Other info: Opportunity for up to 10% travel and a dynamic work environment focused on teamwork.

The predicted salary is between 36000 - 60000 £ per year.

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step. As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Benefits include:

  • Medical, dental and vision insurance
  • Paid time off and company holidays
  • 401(k) retirement plan with company-match
  • Annual incentive program

Summary: The Sub Investigator has responsibility for the clinical safety of the patients partaking in the clinical trial, collecting, and recording accurate clinical data while also ensuring that the well-being and interests of the subjects enrolled in the studies are being met. The Sub-I provides essential clinical support to the clinical research coordinators, principal investigators, and other clinical trials staff.

Responsibilities:

  • Serve as leader of a study team to execute clinical trials
  • Mentor and train staff in the conduct of clinical trials, protocol requirements, communication, and trial management skills
  • Create training strategies and mitigation plans
  • Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
  • Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports
  • Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study
  • Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols
  • Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
  • Ensure good documentation practices are applied by team members when collecting and correcting data, transferring data to sponsor/CRO data capture systems and resolving queries
  • Ensure confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information is maintained by all team members
  • Develop communication and escalation strategies within teams to ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and Velocity SOPs
  • Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner
  • Ensure staff are delegated and trained appropriately and documented
  • Ensure the creation, collection and submission of regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations and IRB requirements
  • Evaluate potential subjects for participation in clinical trials including phone and in person prescreens
  • Create and execute recruitment strategies in conjunction with patient recruitment staff
  • Incorporate key timelines, endpoints, required vendors, and patient population when planning for each assigned protocol
  • Incorporate understanding of how decisions affect the bottom-line including links between operations and company’s financial performance and how it is essential to create value of all stakeholders of the organization when planning for each assigned protocol
  • Incorporate understanding of product development lifecycle and significance of protocol design including critical data points when planning for each assigned protocol
  • Develop Quality Control strategies for team member projects
  • Perform clinical duties (e.g. Drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
  • Promote respect for cultural diversity and conventions with all individuals
  • Understand the disease process or condition under study
  • Other duties as assigned

Qualifications:

  • Must be licensed as a MD, DO, NP, or PA in the state you work in
  • Must undertake all training and certification required by sponsors and CRO’s to carry out clinical trials within specified timelines
  • Safe handling of data and records regarding privacy and confidentiality, per HIPAA requirements
  • Practices professionalism and integrity in all actions – Demonstrated ability to foster concepts of teamwork, cooperation, self-control, and flexibility to get the work done
  • Ability to communicate effectively in English (both verbal and written)
  • Up to 10% travel, as needed, for project team meetings, client presentations and other professional meetings/conferences as needed
  • Other duties as assigned

Education and Experience:

  • Must be a licensed MD, DO, NP, or PA
  • 5+ years of clinical management experience or equivalent applicable experience in clinical research industry

Physical Requirements:

  • Prolonged periods of sitting at a desk and working on a computer
  • Must be able to lift up to 15 pounds at times

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

Sub Investigator employer: Velocity Clinical Research, Inc.

Velocity Clinical Research is an exceptional employer that prioritises employee growth and development, offering comprehensive benefits such as medical, dental, and vision insurance, alongside a 401(k) retirement plan with company matching. Our collaborative work culture fosters innovation and excellence in clinical trials, ensuring that every team member plays a vital role in delivering high-quality patient care while advancing their careers in a supportive environment.
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Contact Detail:

Velocity Clinical Research, Inc. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Sub Investigator

✨Tip Number 1

Familiarise yourself with the latest clinical trial regulations and guidelines, such as GCP and ICH. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.

✨Tip Number 2

Network with professionals in the clinical research field, especially those who have experience as Sub Investigators. Attend industry conferences or local meetups to build connections that could lead to job opportunities at Velocity.

✨Tip Number 3

Showcase your leadership skills by discussing any previous experiences where you mentored or trained staff. Highlighting these experiences can set you apart as a candidate who can effectively manage a study team.

✨Tip Number 4

Prepare to discuss your understanding of patient safety and ethical considerations in clinical trials. Being able to articulate how you prioritise patient well-being will resonate well with Velocity's mission and values.

We think you need these skills to ace Sub Investigator

Clinical Management Experience
Knowledge of GCP and ICH Guidelines
Patient Safety Awareness
Data Collection and Documentation Skills
Regulatory Compliance Knowledge
Adverse Event Reporting
Project Management Skills
Effective Communication Skills
Team Leadership and Mentoring
Recruitment Strategy Development
Understanding of Clinical Trial Protocols
Confidentiality and Privacy Practices
Problem-Solving Skills
Flexibility and Adaptability
Professionalism and Integrity

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant clinical management experience and any specific qualifications such as being a licensed MD, DO, NP, or PA. Emphasise your experience in clinical trials and patient care.

Craft a Strong Cover Letter: In your cover letter, express your passion for clinical research and how your skills align with Velocity's mission. Mention specific experiences that demonstrate your ability to manage clinical trials and ensure patient safety.

Highlight Relevant Skills: Clearly outline your skills related to clinical trial management, communication, and teamwork. Mention your understanding of GCP, ICH Guidelines, and any project management concepts you have applied in previous roles.

Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects professionalism and attention to detail, which are crucial in the clinical research field.

How to prepare for a job interview at Velocity Clinical Research, Inc.

✨Understand the Role Thoroughly

Before the interview, make sure you have a solid understanding of the Sub Investigator role. Familiarise yourself with clinical trial processes, GCP, ICH guidelines, and the specific responsibilities outlined in the job description. This will help you answer questions confidently and demonstrate your knowledge.

✨Showcase Your Experience

Be prepared to discuss your previous clinical management experience or any relevant roles you've held. Highlight specific examples where you've successfully managed trials, mentored staff, or implemented quality control strategies. This will illustrate your capability to handle the responsibilities of the position.

✨Emphasise Communication Skills

Effective communication is key in this role. Be ready to provide examples of how you've communicated with various stakeholders, including study subjects, sponsors, and team members. Demonstrating your ability to convey complex information clearly will be crucial.

✨Prepare Questions for the Interviewers

Having thoughtful questions prepared shows your interest in the role and the company. Ask about their approach to patient care, how they support career advancement, or what challenges they currently face in clinical trials. This not only helps you gauge if the company is the right fit but also engages the interviewers.

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