2

Pharmaceutical Neurology Remote Jobs (NOW HIRING)

Neurology Account Manager

Seattle, WA · On-site +1

$140K - $160K/yr

Neurology Account Manager - Full time, remote position covering the Pacific North West Cycle ... The Opportunity Cycle Pharmaceuticals is recruiting for a Rare Disease Account Manager to join our ...

Neurology Account Manager

Seattle, WA · On-site +1

$140K - $160K/yr

Neurology Account Manager - Full time, remote position covering the Pacific North West Cycle ... The Opportunity Cycle Pharmaceuticals is recruiting for a Rare Disease Account Manager to join our ...

next page

Showing results 1-20

Pharmaceutical Neurology Remote information

See salary details

$83.5K

$347.7K

$400K

How much do pharmaceutical neurology remote jobs pay per year?

As of Jul 26, 2026, the average yearly pay for pharmaceutical neurology remote in the United States is $347,715.00, according to ZipRecruiter salary data. Most workers in this role earn between $320,500.00 and $400,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Neurology Remote professional, and why are they important?

To excel in a Pharmaceutical Neurology Remote role, you typically need a background in neuroscience, pharmacology, or related life sciences, along with experience in pharmaceutical research or clinical trials. Familiarity with clinical trial management systems, data analysis tools, and regulatory compliance platforms is crucial. Strong communication, attention to detail, and self-motivation are essential soft skills for effective collaboration and independent work in a remote setting. These competencies ensure accurate research, regulatory adherence, and seamless coordination across teams, which are vital for advancing neurological therapies.

What is the difference between Pharmaceutical Neurology Remote vs Pharmaceutical Neurology On-site?

AspectPharmaceutical Neurology RemotePharmaceutical Neurology On-site
Work EnvironmentRemote, home-based setting with virtual collaborationOn-site, in-office or clinical setting with direct supervision
Required CredentialsPharmacy or medical degree, relevant certifications, strong communication skillsSame as remote, with additional in-person training or meetings
Employer & Industry UsagePharmaceutical companies, telehealth providers, medical communication firmsHospitals, clinics, pharmaceutical companies with on-site teams
Work TasksConsultations, medical education, remote patient supportIn-person patient interactions, clinical assessments, team meetings

Pharmaceutical Neurology Remote roles focus on virtual patient support and medical communication, offering flexibility and home-based work. On-site positions involve direct patient care and team collaboration in clinical settings. Both roles require similar credentials but differ mainly in work environment and daily tasks.

How does a remote pharmaceutical neurology professional collaborate effectively with cross-functional teams?

As a remote pharmaceutical neurology professional, you'll frequently collaborate with clinical researchers, regulatory experts, and medical affairs teams through virtual meetings, shared project management platforms, and regular status updates. Effective communication and proactive calendar management are essential to stay aligned on project goals, timelines, and data sharing. Building strong digital relationships and leveraging collaboration tools can help overcome the challenges of not being physically present, ensuring you remain an integral part of the team and contribute meaningfully to drug development and clinical trial success.

What is a pharmaceutical neurology remote job?

A pharmaceutical neurology remote job involves working from a location outside of a traditional office, typically from home, to support the development, testing, and marketing of medications related to neurological conditions. Professionals in this field may work in clinical research, medical affairs, regulatory affairs, or sales roles for pharmaceutical companies that specialize in neurology. Responsibilities can include conducting virtual clinical trials, liaising with healthcare providers, reviewing scientific data, and assisting with regulatory submissions—all focused on neurological treatments. Remote roles allow for greater flexibility and often use digital tools to collaborate with team members and clients globally. These positions require a strong background in neuroscience or pharmaceuticals, as well as excellent communication and technical skills.
More about Pharmaceutical Neurology Remote jobs
What cities are hiring for Pharmaceutical Neurology Remote jobs? Cities with the most Pharmaceutical Neurology Remote job openings:
What states have the most Pharmaceutical Neurology Remote jobs? States with the most job openings for Pharmaceutical Neurology Remote jobs include:
Infographic showing various Pharmaceutical Neurology Remote job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 87% Full Time, 8% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $347,715 per year, or $167.2 per hour.
Medical Director, Clinical Trial Physician - Neurology (Remote) - FSP

Medical Director, Clinical Trial Physician - Neurology (Remote) - FSP

Thermo Fisher Scientific

NC • Remote

Full-time

Posted 14 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 419 frontline employees who took The Breakroom Quiz

200th of 535 rated manufacturers


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
Location/Division Specific Information

Join Thermo Fisher Scientific as a Medical Director/Clinical Trial Physician(FSP) based in the United States and be part of a world-class organization conducting groundbreaking research. Ideal candidate location is Eastern or Central Time Zone. This position is fully remote, benefit eligible with travel in a 10-20% range(international maybe required).

*Must be legally authorized to work in the United States or Canada without sponsorship.

*Must be able to pass a comprehensive background check, which includes a drug screening(where applicable).

*East coast time zone is preferred, or ability to work EST hours

Client Dedicated Role:

Our client, a global mid-sized biotech company, focuses on developing innovative treatments for patients with autoimmune diseases. This fast-growing, international organization has a strong scientific foundation. If you're looking for a place where your work, in partnership with others, can have real impact—and where you're encouraged to challenge yourself and contribute to breakthrough solutions , the Medical Director/Clinical Trial Physician could be a great fit.

Discover Impactful Work:

Provides clear medical leadership in the Study team, working in close collaboration with the other members of this cross functional team, in order to provide reliable, high quality study data within time and budget.

A day in the Life:
  • Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, contribute to review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials

  • Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active escalation and correction of issues in consultation with the Global Medical Indication Lead

  • Interpret the clinical trial data for regulatory documents (e.g. CSR, INDs, Annual Reports, NDAs, MAAs, etc.), manuscripts, and other publications as required, in consultation with the Indication Lead

  • Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications

  • Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP

  • Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties

  • In case more than 1 physician is working on the protocol, a primus inter pares will be appointed, and they will ensure that answers to questions from sites /IRBs RAs, eligibility and protocol deviation decisions will be harmonized across medics

Keys to Success:Education
  • Medical Doctor or equivalent degree required. Board certification(s) are preferred

  • Specialty education(e.g. residency/fellowship) required in neurology. This should be accompanied by patient treatment and/or research experience

  • 1-3 years of industry experience required. Experience should be in clinical development in a Pharmaceutical, Biotech or CRO organization

  • Neurologists with expertise in Pediatric Neurology or Neuromuscular diseases are highly preferred.

Knowledge, Skills, Abilities
  • Excellent English, both written and spoken is a must, as well as ability to travel

  • Shown understanding and experience with NDA submission process

  • Shown understanding of regulatory guidelines for adverse event reporting

  • Proven interpersonal skills enabling to lead a study team, while recognizing individual expert competencies, providing medical advice and evaluations exercising judgment in which issues need to be escalated immediately

  • Pro-active problem solver with negotiation skills, remaining sensitive to the different cultural needs in a global organization

  • Strong communication skills to ensure close collaboration with the cross functional team members so that study plans and status are transparent, and that risks, issues, and results are clear to all involved parties. A matrix structure requires additional skills in gathering decision information, negotiation and communicating decisions and actions

Physical Requirements / Work Environment
  • Work is performed in an office environment with exposure to electrical office equipment

  • Occasional drives to site locations with occasional travel both domestic and international

  • Frequently stationary for 6-8 hours per day

  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists

  • Frequent mobility required

  • Occasional crouching, stooping, bending and twisting of upper body and neck

  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf

  • Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences

  • Frequently interacts with others to obtain or relate information to diverse groups

  • Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration

  • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task

  • Regular and consistent attendance

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!


What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom