Investigator, MD / DO

Headlands Research; Kelowna; On-site; CAD 90,000 - 130,000; Full time

Job summary

A clinical research organization in Kelowna seeks a physician to support their clinical trials. The role offers flexible scheduling and a collaborative environment, focusing on enhancing trial delivery. Previous clinical research experience is a plus, but candidates with the necessary medical licenses are encouraged to apply. This position is onsite in Kelowna, BC, with responsibilities including leadership of site staff and ensuring compliance with clinical trial protocols.

Benefits

Flexible Schedule

Dynamic Team Environment

Qualifications

• Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials is a huge plus.
• Eligible for or active unencumbered license to practice as an MD or DO within British Columbia.
• Must be board-certified or board-eligible.

Responsibilities

• Assist the Principal Investigator with conducting clinical trials.
• Provide leadership and mentorship to site staff.
• Oversee subject safety and ensure compliance with protocols.

Skills

Leadership skills

Excellent communication

Organizational skills

Knowledge of GCP guidelines

Education

MD or DO license in British Columbia

Board-certified or board-eligible

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.

Join Us in Improving Lives through Clinical Research

At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us—it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.

The Role of a Lifetime

Are you ready to make a difference? We're seeking an experienced physician to help us grow our clinical Okanagan Clinical Trials research site located in Kelowna, BC. We are open to a variety of specialties - Internal Med, Emergency Med, Urgent Care, Family Practice, Endocrinology, Infectious Disease... We are flexible in our need and want to speak with you if you are interested in full-time or part-time commitments.

Why Join Us?

• Flexible Schedule: Work on your terms, with a schedule that fits your life.
• Dynamic Team Environment: You'll help Headlands Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.
  
  

Type: Part-time or Full-time Employee

Pay: Competitive and dependent upon years of experience as an Investigator in clinical research.

Location: Onsite in Kelowna, BC (no opportunities for remote or hybrid)

Responsibilities

• Assist the Principal Investigator with conducting clinical trials at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
• Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
• Participate in investigator meetings(when necessary and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
• Obtain IRB approval for study initiation and any protocol modifications.
• Oversee subject safety, trial conduct compliance, and the informed consent process.
• Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
• Provide ongoing training and support to research staff.
  
  

Qualifications

• Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.
• Eligible for or active unencumbered license to practice as an MD or DO within the province of British Columbia required
• Must be board-certified or board-eligible.
• Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
• Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
• Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.