Clinical Research Physician - Part Time Opportunity! at Thermo Fisher Scientific

Atlanta, Georgia, United States

Apply Now

Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Part TimeJob Type

NoVisa

Clinical Research, Biopharmaceutical, HealthcareIndustries

Requirements

Valid medical degree and registration within the country of practice
Medical license in good standing, with unrestricted ability to practice in place of work (where applicable)
Valid ICH GCP certificate (can be obtained after employment)
Exceptional general medical practitioner diagnosis and treatment proficiency
At least one-year experience working in clinical research, or comparable research/clinical expertise to demonstrate the ability to work in clinical trials (or equivalency of appropriate education, training, and/or directly related experience)
Good understanding of medical terminology, drug safety, and interpretation of lab reports
Computer proficiency and confident in using Microsoft Office and other sponsor-related programs and portals
Legally authorized to work in the United States without sponsorship
Ability to pass a comprehensive background check, including drug screening

Responsibilities

Conducts all clinical trials (studies) according to ICH GCP, local regulations, study protocol, and company processes
Ensures the medical wellbeing and safety of participants through safe performance and execution of studies
Maintains clinical oversight and quality on studies, delivering on study targets including recruitment, enrolment, and retention of participants
Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies
Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants
Interprets protocols and Investigator's Brochure (IB) and participates in initiatives to strategize for patient recruitment
Ensures and protects the welfare and safety of participants through ethical conduct (highest priority at all times)
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 actions complaints or Quality Issues (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 product (IMP)

Skills

Key technologies and capabilities for this role

ICH GCPclinical trialsstudy protocolpatient safetyclinical oversightGCP compliancelocal regulationsbiopharmaceutical researchpatient enrollmentsite performance

Questions & Answers

Common questions about this position

Is this a full-time or part-time position?

This is a part-time position with approximately 26 hours per week.

What is the work schedule for this role?

The schedule is standard Monday through Friday during the day, approximately 26 hours per week.

What skills and qualifications are required for the Clinical Research Physician role?

Candidates must be legally authorized to work in the United States without sponsorship, able to pass a comprehensive background check including drug screening, and experienced in conducting clinical trials according to ICH GCP, local regulations, study protocols, with skills in participant evaluation, safety oversight, protocol interpretation, and audit preparation.

What does a typical day look like for this position?

A typical day involves carrying out clinical evaluations of participants, reviewing enrollment progress and screening rates, interpreting protocols for patient recruitment, ensuring participant safety and ethical conduct, complying with medical duties per protocol and regulations, reporting safety threats, and preparing for audits.

What is the location requirement for this job?

The position is office-based, with more than 150 clinical research sites located throughout the world via Trialmed.

Thermo Fisher Scientific

Provides life sciences products and services

About Thermo Fisher Scientific

Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.

Waltham, MassachusettsHeadquarters

1956Year Founded

$17MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Increased competition in single-use bioprocessing may impact market share.

Sale of anatomical pathology business could create a temporary product gap.

Investment in miDiagnostics may face regulatory challenges affecting returns.

Differentiation

Thermo Fisher offers a comprehensive range of life sciences products and services.

Their well-known brands include Thermo Scientific, Applied Biosystems, and Invitrogen.

They provide strong customer support and educational resources to optimize client workflows.

Upsides

Expansion of biologics production facility enhances capacity for precision biologics monitoring.

Investment in miDiagnostics aligns with demand for rapid diagnostic solutions in BioPharma.

Collaboration with Mainz Biomed positions them in the growing cancer detection market.

Land your dream remote job 3x faster with AI

Try Jobo Free