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Medical Director / Senior Medical Director, Psychiatry

74-2325267 PPD Development, LP

LocationUnited States
SeniorityMedical Director or Senior Medical Director
Company74-2325267 PPD Development, LP
Verified recentlyChecked today
Compensation

Salary not listed

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Requirements and working style

Decision details from the source listing

Experience

2-2 years stated

Education

MD or equivalent required, Formal psychiatry training, such as residency and/or fellowship

Visa sponsorship

Listed as unavailable

Work authorization

Must be legally authorized to work in the hiring country without sponsorship

Schedule

fixed

Benefits stated
Annual incentive plan bonusHealthcareOther employee benefitsCareer and development prospects

These fields are normalized from the employer's text. Confirm details on the employer site before applying.

WFH.team analysis

What this posting tells you

Remote US Medical Director/Senior Medical Director role providing medical oversight for psychiatry clinical trials, including safety review, medical consultation, and clinical data review. Requires an MD or equivalent, formal psychiatry training, and patient treatment experience comparable to at least two years. Senior-level candidates should also have approximately 1–2 years of relevant clinical trial industry experience. Must be authorized to work in the hiring country without sponsorship. Schedule is standard Monday–Friday; salary is not stated.

Role lane

Customer success, Data, Education, Healthcare admin, Medical billing, Operations, Patient support, Product, Sales, Software, Customer support

Where you can work

United States

Working hours

Global

Arrangement

Medical Director or Senior Medical Director · contract · full_time

Required signals
Psychiatry therapeutic expertiseClinical experience in psychiatryFormal psychiatry trainingPatient treatment experienceClinical trial medical oversightGood Clinical Practice and ICH guidelinesSafety and adverse event reviewClinical data reviewMedical judgment and decision-makingWritten and oral communicationEnglish fluency
Preferred signals
Active medical licensureClinical trial experience in a CRO or pharmaceutical companyClinical development or medical monitoring experienceWorking knowledge of MedDRA or relevant safety databasesBiostatisticsData managementClinical operations proceduresFDA, EMA, and GCP guidelines
Confirm before applying
  • Compensation is not listed
Market context

Customer success hiring on WFH.team

6,743active related roles
4,144new in the latest period
2697.2jobs per 100 candidates
$123kmedian of comparable listed ranges

Category counts come from WFH.team's latest published remote job market snapshot.

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Skills and signals
Psychiatry therapeutic expertiseClinical experience in psychiatryFormal psychiatry trainingPatient treatment experienceClinical trial medical oversightGood Clinical Practice and ICH guidelinesSafety and adverse event reviewClinical data reviewMedical judgment and decision-makingWritten and oral communicationEnglish fluencyActive medical licensureClinical trial experience in a CRO or pharmaceutical companyClinical development or medical monitoring experienceWorking knowledge of MedDRA or relevant safety databasesBiostatisticsFully remote; listing identifies the United States and Texas/Austin as remote locations.
Job description

Medical Director / Senior Medical Director, Psychiatry at 74-2325267 PPD Development, LP

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Location/Division Specific Information

Our detailed, goal-oriented Medical colleagues manage the safety profile of new drugs in clinical trials. As part of your work with beginning-to-end trial experience, you will expand your knowledge and experience working on clinical trials through every stage of drug development. This includes management and oversight of all contracted services.

*Must be legally authorized to work in the hiring country without sponsorship.

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

Discover Impactful Work

The Medical Director/Senior Medical Director Psychiatry position provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities, and provides medical review and analysis for clinical trial serious adverse events

A day in the Life

General Support

  • Ensures tasks delegated to medical monitors are properly executed. Adheres to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Adheres to client SOPs/directives and project specific WPDs for assigned projects. Adheres to PPD’s corporate policies and SOPs/WPDs.
  • Provides medical consultation to team members and answer all study related medical questions. Communicates clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately.
  • Provides therapeutic training and protocol training on assigned studies, as requested.

Clinical Trial Support

  • Monitors all safety variables (AE, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medication for protocol restrictions, and un-blinding requests) of clinical studies.
  • Discusses all medical concerns with principal investigators and clients (e.g.discussion regarding interpretation of inclusion/exclusion criteria) raised during the course of a study, using proper medical judgment in the interpretation and decision making with regard to clinical situations as they relate to the investigational study.
  • Provides medical review of adverse events of special interest, serious adverse events and clinical outcomes events reported by study sites.
  • Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess for potential safety concerns.

Keys to Success

Education and Experience

  • MD or equivalent required. Active medical licensure preferred but not required. Candidates should have clinical experience in Psychiatry and formal training in Psychiatry (i.e residency and/or fellowship), along with patient treatment experience (comparable to 2 years).

For Senior Medical Director Level

  • Candidates should have a combination of clinical experience as above and industry experience as follows:
  • Suitable clinical trial experience in a Contract Research Organization or pharmaceutical company (comparable to 1-2 years) in the industry
  • Preference towards individuals with clinical development/medical monitoring experience

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Job leveling at Medical Director or Senior Medical Director will be determined during the consideration process, inclusive of education, experience, therapeutic area(s), and interview results.

Knowledge, Skills and Abilities

  • Therapeutic expertise in Psychiatry
  • Strong decision-making, problem solving, organizational skills and analytical skills
  • Excellent oral and written communication skills
  • Working knowledge of relevant safety databases (e.g. Meddra)
  • Flexibility to travel domestically and internationally
  • Ability to work independently, analyze work with attention to detail, process and prioritize sensitive complex information
  • Proficiency in basic computer applications
  • Fluent in spoken and written English
  • Excellent interpersonal, influencing and team building skills
  • Understanding guidelines (FDA, ICH, EMA and GCP)
  • Working knowledge of biostatistics, data management, and clinical operations procedures
  • Ability to act as a mentor/trainer to other staff

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!

Why join us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Company context

Working remotely at 74-2325267 PPD Development, LP

74-2325267 PPD Development, LP is hiring for 12 active remote roles, with remote-friendly openings, application links, and job details refreshed from the public remote job inventory.

Remote policy

Remote hiring signal is inferred from active confirmed-remote job listings.

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