Physician, MD/DO - Clinical Research - Part-time
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.
📍 Location: Maplewood, MN | 🏥 Site Name: Headlands Research - Twin Cities | 🕒 Part-Time | 🧪 Clinical Research
Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
Type: Regular Part-time Employee or 1099 Independent Contractor
Schedule: Site hours are Mondays through Fridays, 8:00am - 5:00pm; specific schedule is TBD.
Location: Onsite in Maplewood, MN (no capabilities for remote or hybrid work)
Reports to: Site Director
💼 What We Offer
- Competitive pay + annual performance incentives
- 401(k) plan with company match for full-time employees
- Company holidays
- A mission-driven culture focused on advancing medicine and improving patient outcomes
🚀 Why Join Us?
You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.
Responsibilities:
- Lead and oversee clinical trials, 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 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.
Requirements:
- Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.
- Nephrologist and Psychiatrist preferred, but open to considering a wide variety of specialties who can oversee outpatient-based pharma clinical research trials.
- Current and unencumbered license to practice as an MD or DO within the state of Minnesota required (or eligible for).
- 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.
Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Skills
As published by greenhouse · 26 questions
Basics
First Name, Last Name, Email, Phone, Resume/CV, Cover Letter
Short answers (10)
- Preferred First Name optional
- Legal First Name
- Legal Last Name
- Mailing Address: County (NOT country)
- Mailing Address 1
- Mailing Address: City
- Mailing Address: Zip Code
- If you do have relatives who currently work at Headlands Research or any of its subsidiaries, please list their full legal name. optional
- How many years of experience do you have in the clinical trials research industry?
- What are your salary or pay expectations?
Pick from a list (16)
- Mailing Address: State/Province/Territory
- Mailing Address: Country
- Have you ever been employed or contracted with Headlands Research or any of its entities? Note: If you are a current employee of Headlands Research, please apply using our Internal Careers Page on the intranet.
- Do you have relatives who currently work at Headlands Research or any of its subsidiaries?
- Please select the highest level of education you have completed.
- Are you legally authorized to work in the country in which this position is posted? (Answer Yes if you are a citizen, green card holder, or currently possess a valid visa/EAD. Answer No if you are on any visa.)
- Will you now or in the future require visa sponsorship? (Answer Yes if your current authorization is temporary or tied to a specific employer and you will need the company to petition for a new visa, like an H-1B, for you to work long-term)
- Are you 18 years of age or older? If "No", offer for regular employment is subject to verification and legal minimum age requirements, and possibly parental consent. As a condition of employment, you will be required to submit proof of age/identity.
- Do you have a current and valid license as an MD or DO in the state/province in which this position is located?
- Has your license to practice in any state ever been suspended, revoked, voluntarily or involuntarily surrended, been subject to a consent or stipulation order, not renewed, denied renewal, or has probation ever been invoked?
- Have you ever been denied membership or renewal thereof, or been subject to disciplinary action in any medical organization?
- Have you ever been subject to a Professional Liability Claim?
- Are you currently board-certified or board-eligible?
- Have your board certifications ever been suspended, revoked, not renewed, denied renewal, or voluntarily or involuntarily surrendered?
- Do you have experience starting IVs?
- Have you ever served as a principal or sub-investigator on any clinical research trial? (Not a requirement.)