New · posted Nov 11
Thermo Fisher Scientific · Pharmaceuticals
Clinical Research Physician Investigator - Part Time
- San Antonio, TX
- On-site
- Part-time
- Senior & Principal
The role
Conducts all clinical trials (studies) according to ICH GCP, local regulations, study protocol and company processes. Ensures the medical wellbeing and safety of the participants through the safe performance and execution of the studies. Drives clinical oversight and quality of the studies at the site, or with PI oversight at other sites. Works as part of a team, with focus on positive interactions with sponsors, clients and staff members at the site. Participates and engages in driving delivery of study targets, thereby contributing to the commercial success of the site which includes: recruitment, enrolment and retention of study participants. Focuses on own development of skills and expertise and assists with training, mentoring and general support to junior physicians. Generally takes on a more active role giving input into the site processes and sharing best practices gained form years of experience. Manages and oversees various studies simultaneously with the responsibility of PI and sub-I.
- Must be legally authorized to work in the United States without sponsorship. This is an onsite position in San Antonio; relocation assistance is not provided.
- Must be able to pass a comprehensive background check, which includes a drug screening.
- This is a part-time position with 22 hours a week total expected. Ideally M-F 8:30am-1pm CST. Some flexibility maybe required.
What you need
- A valid medical degree within the country of practice with at least 3 years working as a licensed physician, as well as other medical licenses as may be required within the country (e.g. dispensing license)
- Valid registration as a medical practitioner, with a medical license in good standing and with unrestricted ability to practice in place of work, where applicable
- Prior clinical research experience is preferred but not required. Candidates should possess sufficient clinical expertise and medical judgment to safely conduct protocol-driven clinical research and oversee study participants. Strong clinical backgrounds seeking to transition into clinical research are encouraged to apply
- A valid ICH GCP certificate(can be obtained after employment)
- Exceptional general medical practitioner diagnosis and treatment proficiency
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, and Abilities:
- Exceptional understanding of medical terminology, drug safety, and interpretation of lab reports
- Thorough understanding of scientific concepts related to the design and analysis of clinical trials
- Excellent written, verbal and presentation skills
- Capable of working well under pressure
- Capable of effectively prioritizing and managing multiple projects
- Strong planning, organizational and project management skills
- Capable of managing outside agencies in order to fulfill project objectives
- Self-starter with ability to thrive under pressure in a fast paced environment
- Skilled in Word, Excel, and PowerPoint and proficient with the Internet
- Displays strategic leadership by influencing the site team to deliver on targets
Working Conditions and Environment:
- Work is performed in an office environment with exposure to electrical office equipment.
- Occasional travel.
Physical Requirements
- 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.
What you'll do
- Carries out clinical evaluation and assessment of participants to ensure eligible participants are recruited and monitored for safety and adherence.
- Attends Site Initiation Visits (SIV), Pre-Selections Visits (PSV) and Investigators meetings as required.
- Participates in recruitment initiatives and strategy development to ensure targets are achieved; ensuring recruiting studies enroll according to plan within timelines and targets.
- Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety and retention of participants.
- Interprets protocols and IB.
- Manages and reviews IVRS, CRF/EDC, if applicable.
- Oversees management of investigational medical product (IMP).
- Identifies and reports trends within studies to manage it in light of conduct and outcome.
- Oversees multiple studies and/or studies with higher numbers.
- Cares for and protects the 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, ensuring that clinical trials are performed to acceptable medical, scientific and ethical standards and meet the requirements as per protocol, SOP/COP ICH and local GCP guidelines and regulations.
Where you'll work
San Antonio, TXOn-siteOpen in Maps (opens in a new tab)
More jobs in San Antonio, TXSchedule and working conditions
Days
Standard (Mon-Fri)
Environmental Conditions
Office
Job intelligence
The context around this role
Live data · November 11, 2026
Salary intelligence
How the pay compares
Senior & Principal roles in the US64 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $115,250 | $124,500 | $126,125 |
Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 11, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Research
The general path across 247 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not Thermo Fisher's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 46 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct7
- Collaboration and leadership5
- GMP and compliance3
- Documentation and SOPs3
- Data and digital systems3
- Investigations and CAPA2
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Research work in pharmaceuticals, led by the one this posting names, each linked to the agency or standards body that publishes it.
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trialsNamed in the posting
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- ICHICH E8(R1)(official source, opens in a new tab)General considerations for clinical studies and quality by design in trials
- HHS45 CFR Part 46 (Common Rule)(official source, opens in a new tab)The federal policy for the protection of human research subjects
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- FDA21 CFR 314.80 and 600.80(official source, opens in a new tab)Postmarketing reporting of adverse drug and biologic experiences
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
- ICHMedDRA(official source, opens in a new tab)The ICH medical terminology for coding adverse events and medical history
Company hiring pulse
Thermo Fisher on Regulatory Jobs
- 117
- Open roles
- 117
- Distinct roles
- 52
- Locations
By discipline
- Quality76 62%
- Clinical40 33%
- Regulatory6 5%
By level
- Senior & Principal58 48%
- Associate & Specialist32 26%
- Manager26 21%
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Clinical Research Physician Investigator - Part Time at Thermo Fisher
Open until filled.