Medical Director - Principal Investigator

Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific, youll 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 *Must be legally authorized to work in the United States without sponsorship.
*Must be able to pass a comprehensive background check, which includes a drug screening(where applicable).
Our Austin Clinical Research Unit(CRU) focuses on Phase I and IB trials which represent the first practical tests of a compounds clinical relevance and commercial viability. They are the culmination of years or even decades of research. Moreover, they set the stage for subsequent studies that will ultimately determine your compounds efficacy, safety and positive impact on patients lives. The site also supports some late phase studies and our facility encompasses over 152,000 square feet including on-site laboratories and pharmacies. Late Phase studies also can take place at this facility.
This is a full-time benefit eligible role. Standard day hours(M-F) with a week of call every 8 weeks. On call expectations are light with a couple evening phone calls and minor weekend work.
Discover Impactful Work: The Medical Director conducts all clinical trials (studies) according to ICH GCP, local regulations, study protocol, and company processes and ensures the medical well-being and safety of the participants through the safe performance and execution of the studies. The role maintains clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site which includes: recruitment, enrolment, and retention of study participants.
A day in the Life:
* Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled in studies.

Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.

Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.

Ensures and protects the welfare and safety of participants through ethical conduct; this should receive the highest priority at all times during all aspects of the study.

Fulfills and complies with all medical duties as per protocol, SOP/COP, ICH, GCP, and local regulations.

Reports any safety threats, that may impact stakeholders/participants and action complaints or QIs as per site processes.

Exercises meticulous attention to detail in recording information and source management.

Actively involved in audit preparations and site inspections.

Oversees the management of investigational medical products (IMP).

Keys to Success: Education
* A valid medical degree (M.D. or D.O.)

A medical license in good standing, with unrestricted ability to practice in place of work, where Applicable. Texas State licensure will be required.

Board Certification in respective field preferred.

A valid ICH GCP certificate (this can be obtained upon employment)

Experience
* No previous experience in clinical research is required but is preferred.

Must have general medical practitioner diagnosis and treatment proficiency.

Minimum of 3+ years of leadership, supervisory, or people management experience in a healthcare, clinical, academic, or related environment.

Demonstrated experience leading multidisciplinary teams, managing performance, and developing talent.

Experience with workforce planning, employee engagement, coaching, and conflict resolution preferred.

Prior responsibility for operational, quality, or business performance metrics is preferred.

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.
Knowledge, Skills, Abilities
* Good understanding of medical terminology, drug safety, and interpretation of lab reports

Computer proficiency and confidence in using Microsoft Office and other sponsor-related programs and portals

Good administration skills and a passion for quality and detail

Capable of working well under pressure and meeting deadlines

Good understanding of commercial and financial concepts and the impact thereof on the business

Capable of consistently working well with others and assisting in other areas as needed

Capable of learning new processes and systems quickly

Strong cognitive skills, with the ability to think, read, learn, reason, interpret, and pay attention to detail in daily operations and tasks

Capable of working independently with good prioritization and multitasking skills

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

Occasional travel locally and internationally

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 is required.

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

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

Ability to access and use various computer software developed 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!