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Allucent
Remote - Nationwide

Sr. Medical Director (Neurologist)

Medical AffairsFull-Time

Compensation

Pay not listed

The week · per this posting · weekdays assumed

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Posted 1mo ago

Job Description

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Board-Certified Neurologist to join our A-team (remote).

As Sr. Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent, serving as the medical monitor contact in study protocols to investigators and study sites team regarding protocol related questions and safety of the subjects enrolled. Experience in Neurology is a requirement for this position.

In this role your key tasks will include:

Independently provide medical monitor support to assigned clinical studies, for example answering medical questions from study team and/or site, assist with protocol interpretation and medical review of generated data including but not limited to clinical laboratory data and case report forms as necessary to ensure adherence to the protocol, consistency and scientific validity of the data. When appropriate, and with the necessary support from senior colleagues, assist the Project Manager in discussions with clients on safety issues or concerns that may have arisen

Prepare the Medical Monitoring and other relevant plans for assigned studies conducted by Allucent prior to the start of the study and in accordance to deliverables contracted.

Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events

Assist clinical data management with MedDRA and WHO coding in assigned trials

Assist by reviewing clinical study documents for medical consistency and relevance, with support of senior medical team members if needed, including but not limited to the clinical trial protocol (CTP), the Informed Consent (ICF) and clinical study report (CSR) other safety reports (e. g., DSUR, PSUR)

Assist in the set up and conduct of Data Safety Boards (DSMB, DMB or similar) and Dose escalation meetings (DEC)

Attend, participate and present in Kick-Off, Investigators’ meeting, and other relevant meetings in assigned projects, as requested.

  • Provide 24/7 urgent medical support for medical and safety advice if required
  • Training of project teams on medical aspects of the trial and therapeutic training as required
  • Review of Protocol Deviations
  • Identify study risks and provide input to the Risk plan
  • Review and understand study medical deliverables laid down in the assigned study’s contract with support of senior colleagues and help track budget spent throughout their assigned study(ies)
  • Attends and may need to present at major therapeutic conferences and drug development conferences
  • Assure good communication and relationships with (future) clients

Contribute and take part with support from senior colleagues as needed in client evaluations, visits and bid defenses

To Be Successful You Will Possess

MD degree

Must Be Board-Certified Neurologist

  • Experience as Neurologist with Alzheimer's disease and Parkinson's disease, other neurology and psychiatry experience are key assets
  • Minimum 7-9 years of relevant work experience with solid Neurology expertise

Good Knowledge of GxP

  • Good standing with local, state (in the US), and national licensing and regulatory authorities and certifying bodies
  • GDPR/HIPAA, CFR/CTR/CTD and applicable (local) regulatory requirements understanding
  • Strong written and verbal communication skills including good command of English language
  • Representative, outgoing and client focused
  • Ability to work in a fast-paced challenging environment of a growing company
  • Administrative excellence
  • Proficiency with various computer applications such as Word, Excel, and PowerPoint required

Benefits of Working at Allucent Include

  • Comprehensive benefits package per location
  • Competitive salaries per location
  • Departmental Study/Training Budget for furthering professional development
  • Flexible Working hours (within reason)
  • Opportunity for remote/hybrid* working depending on location
  • Leadership and mentoring opportunities
  • Participation in our Buddy Program as a new or existing employee
  • Internal growth opportunities and career progression
  • Financially rewarding internal employee referral program
  • Access to online soft-skills and technical training via ADP and internal platforms
  • Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
  • Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

Disclaimers

*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles.

Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

Key Responsibilities

The Sr. Medical Director is responsible for ensuring the medical and safety integrity of clinical trials by serving as the medical monitor and providing protocol interpretation. They will also review safety data, assist with clinical study documentation, and support project teams throughout the trial lifecycle.

Requirements

Candidates must hold an MD degree and be a Board-Certified Neurologist with 7-9 years of relevant experience. Proficiency in GxP, regulatory requirements, and strong communication skills are essential for this role.

Qualifications

Education
Doctoral or professional degree (postgraduate degree)
Experience
5+ years of experience

Certifications

Board Certification

Key Skills

Data reviewClinical study reportsRisk managementRegulatory complianceProject managementAlzheimer's disease expertise

Medical Affairs — Physician Career Context

Medical Affairs pay on WeekdayDoc is up 2.9% vs. the prior quarter (through Oct 2026).

Where are Medical Affairs jobs?
MeasureThis jobMarket
Work-life score6.0 / 10 · top 25% in medical affairsranked against 273 Medical Affairs listingslisting-based score, 0–10
Listed paynot listedMedical Affairs median $298k (middle half $264k–$324k)62 comparable listings, Nov 2026
Sign-on & loan repaymentnot statedUS physician listings (all specialties): 26% state a sign-on bonus (median $50k) · 12% offer loan repayment1,000 active listings, Nov 2026
Medical Affairs hiring demand#6 of 28 specialtiespostings stay open a median 69 daysWeekdayDoc Hiring Index, October 2026 · 162 postings, 36 closed
New Medical Affairs listings94 in the last 30 days90 the 30 days before (+4%)U.S., first seen on WeekdayDoc, Nov 2026
Medical Affairs pay trend+2.9% vs prior quarter—through Oct 2026
Sources: WeekdayDoc live listing index (273 Medical Affairs listings), WeekdayDoc Hiring Index; as of Nov 2026. Same values as the Weekday Verdict and Market Insights on this page.

Work-Life Balance Analysis

WeekdayDoc's proprietary algorithm rates Sr. Medical Director (Neurologist) at Allucent a 6.0 out of 10 for work-life balance — classified as good. This places the position in the top 25% in Medical Affairs — ranked against 273 active Medical Affairs listings on WeekdayDoc. Contributing factors include remote work flexibility.

Top Medical Affairs Jobs

1 matches · ranked by pay
#1

Payer & Health Systems Oncology, Medical Affairs Director (PHSO MAD) (PA, MD, Upstate NY)

MSD · Baltimore, Maryland

$210k-$331k

Work-life snapshot

median 3.0this job 6.0
Better work-life than 80% of Medical Affairs listings

Listing-based score, 0–10, across 273 comparable listings. Shaded area = the share scoring below this one.

  • Hybrid
  • Remote
Allucent logo

About Allucent

Pharmaceutical Manufacturing
Cary, North Carolina
1,001-5,000 employees

Benefits & Perks

Comprehensive Benefits Package
Departmental Study/Training Budget
Flexible Working Hours
Remote/Hybrid Work
Leadership and Mentoring Opportunities
Internal Growth Opportunities
Spot Bonus Award Program
Loyalty Award Program