... clinical trial data and other observational databases to develop an understanding of potential ... Remote
... clinical trial data and other observational databases to develop an understanding of potential ... Remote
Remote Clinical Trial information
See Rochester, MN salary details
$29.32 - $35.54
4% of jobs
$35.54 - $41.76
6% of jobs
$41.76 - $47.98
7% of jobs
$52.65 is the 25th percentile. Wages below this are outliers.
$47.98 - $54.20
9% of jobs
$54.20 - $60.42
15% of jobs
The median wage is $63.16 / hr.
$60.42 - $66.64
18% of jobs
$71.07 is the 75th percentile. Wages above this are outliers.
$66.64 - $72.86
21% of jobs
$72.86 - $79.08
7% of jobs
$79.08 - $85.30
6% of jobs
$85.30 - $91.52
3% of jobs
$91.52 - $97.74
2% of jobs
$29
$63
$97
How much do remote clinical trial jobs pay per hour?
What is a Remote Clinical Trial job?
A Remote Clinical Trial job involves managing or supporting clinical research studies from a remote location rather than on-site at a hospital or research facility. Responsibilities may include data management, patient monitoring, regulatory compliance, and coordinating trial activities. These roles are often held by clinical research associates, coordinators, or data analysts who use digital tools to oversee the trial process. Remote roles help improve accessibility and efficiency while maintaining compliance with regulatory standards.
What are the key skills and qualifications needed to thrive in the Remote Clinical Trial position, and why are they important?
To thrive in a Remote Clinical Trial position, you need a strong background in clinical research, regulatory compliance, and data management—often supported by a degree in life sciences or health-related fields. Familiarity with electronic data capture (EDC) systems, clinical trial management software (CTMS), and certifications like GCP (Good Clinical Practice) are highly beneficial. Exceptional organizational skills, attention to detail, and proactive communication are essential soft skills for remote collaboration and project management. These abilities ensure accurate trial execution, compliance with protocols, and seamless teamwork across distributed environments.
What are some common challenges faced in remote clinical trial roles, and how can they be managed?
One of the main challenges in remote clinical trial roles is maintaining effective communication and collaboration with research teams, participants, and stakeholders across various locations. This can be managed by utilizing secure collaboration tools, scheduling regular virtual check-ins, and following clear documentation practices. Remote professionals may also face difficulties in monitoring protocol compliance and data integrity without onsite presence, making strong organizational skills and familiarity with virtual monitoring tools essential. Being proactive and adaptable helps you address issues promptly and ensures study milestones are met. With the right support and resources, remote clinical trial professionals can seamlessly contribute to successful trial outcomes.
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 17 days ago
Johnson & Johnson rating
8.0
Based on 100 frontline employees who took The Breakroom Quiz
35th of 71 rated pharmaceutical
Job description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Epidemiology
Job Category:
People Leader
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for the role of Associate Director, Oncology Epidemiology. We have a preference for this position to be located in either Raritan, NJ or Horsham, PA. Remote work options in the US may be considered on a case-by-case basis and if approved by the Company.
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in this role will also function under the supervision of more senior members of the department.
Primary responsibilities:
- Assist with identifying research study needs, drafting proposals and protocols, and contributing to epidemiology strategy and study conduct across the clinical development program.
- May conduct fit for purpose database and study feasibility assessments and execute analyses across the product cycle.
- Conduct literature reviews and synthesis; provide assistance to clinical teams with study design; and identify and evaluate data resources to meet therapeutic needs.
- Work closely with colleagues in the Observational Health Data Analytics group when defining research questions, developing epidemiological protocols, and implementing solutions.
- Provide epidemiological and/or statistical consulting, education and support to product teams, and disseminate technical information through technical reports, presentation, and publication in peer-reviewed literature, as agreed by the team.
- Research natural history of diseases, both within and outside of existing electronic databases, to understand the inherent risks associated with the indication; statistical risk assessment; using historical clinical trial data and other observational databases to develop an understanding of potential safety issues for new medications, and indications, based on experience with related compounds.
- May work in cross departmental/sector committees, and or other efforts supporting J&J Innovative Medicine.
- Keep up to date with the FDA and other Regulatory Agencies regarding regulatory requirements for Post Approval Authorization Studies and Risk Management plans and the development of formal guidance for use of RWE for Regulatory Decision Making.
Qualifications:
- PhD in Epidemiology or a closely related field OR MD with training and degree in Epidemiology or a closely related field OR Master’s degree with at least 4 years of hands-on experience is required.
- At least 3 years of Epidemiology research experience is required.
- Must have an understanding and the ability to interpret quantitative methods.
- Experience with writing observational study protocols, proposals, and/or proposal requests, particularly the methods sections, is required.
- A track record of authoring scientific communications (peer-reviewed publications, poster or oral presentations at conferences, technical reports) is required.
- Experience working with large administrative or medical records databases is preferred.
- Applied pharmacoepidemiology research is preferred.
- Background in epidemiologic material on specific diseases, conditions, or therapies particularly relating to Oncology therapeutic area is preferred.
- Experience working with health authorities is preferred.
- Phase III/IV medicine development experience is preferred.
- Experience working in a global environment is preferred.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.
We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
The anticipated base pay range for this position is $137,000 to 235,750. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
Employees are eligible for the following time off benefits:
Vacation – up to 120 hours per calendar year
Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year
Holiday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar year
Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits
The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.
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