Home › Companies › Alcanzaclinical › Clinical Research Physician - Metabolic or Hepatology - part time (16 hours per week)
Clinical Research Physician - Metabolic or Hepatology - part time (16 hours per week)
Alcanzaclinical · Olympus - Sugar Land, TX, Sugar Land, Texas · On Site · Active · Pinpoint
Job facts
| Field | Value |
|---|---|
| Company | Alcanzaclinical |
| Title | Clinical Research Physician - Metabolic or Hepatology - part time (16 hours per week) |
| Normalized title | - |
| Department / team | Operations |
| Location | Olympus - Sugar Land, TX, United States |
| Work model | On Site |
| Employment type | Part Time |
| Salary | 0-0 |
| Status | active |
| ATS provider | Pinpoint |
| Posted / first seen | — / 2026-05-31 |
| Changed / last seen | 2026-05-31 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Alcanzaclinical. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Pinpoint. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Olympus - Sugar Land. | Open |
| Department jobs | Active postings in Operations. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Alcanzaclinical |
| Source | 475d8ecd-9e61-4c5b-8d96-44eb7fb8578b |
| ATS provider | Pinpoint |
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.
Essential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance Evaluates and assesses participants to ensure only eligible participants enroll into the trials. Participates and engages in successful delivery and retention of study participants. Interacts positively and collaboratively with sponsors, clients and team members. Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs. Actively involved in protocol training for staff. Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues. Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role. Clinical research experience is required. Board certification in area of specialty required. CPR required / ACLS preferred.
Required Skills: Clinical skills and clinical procedures based on area of specialty. Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm). Must possess strong organizational skills, attention to detail, and math proficiency. Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred. Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers. Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities. Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic. Must possess a high degree of urgency, self-motivation, integrity and dependability. Ability to work independently to identify problems and implement solutions. Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
Full job record
| Job ID | 58f86fac22ca17e13bb643a30caa73ecbeeb5f9a |
| Org ID | 82cff78a-f68b-4a7b-9bc0-5a37dd8a10b7 |
| Source ID | 475d8ecd-9e61-4c5b-8d96-44eb7fb8578b |
| Board ID | 475d8ecd-9e61-4c5b-8d96-44eb7fb8578b |
| Provider | pinpoint |
| Provider Job Key | 456820 |
| Title | Clinical Research Physician - Metabolic or Hepatology - part time (16 hours per week) |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Olympus - Sugar Land, TX, Sugar Land, Texas |
| Department | Operations |
| Team | — |
| Employment Type | part_time |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | United States |
| Region | TX |
| City | Olympus - Sugar Land |
| Salary Raw | 0-0 |
| Salary Min | 0 |
| Salary Max | 0 |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://alcanzaclinical.pinpointhq.com/en/postings/158080b5-9924-4a8b-a41f-a68b8e13efe2 |
| Apply URL | https://alcanzaclinical.pinpointhq.com/en/postings/158080b5-9924-4a8b-a41f-a68b8e13efe2 |
| First Seen At | 2026-05-31 17:45:56Z |
| Last Seen At | 2026-06-06 20:05:25Z |
| Last Checked At | 2026-06-06 20:05:25Z |
| Last Changed At | 2026-05-31 17:45:56Z |
| Inactive At | — |
| Source Posted At | — |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=pinpoint/board=alcanzaclinical/date=2026-06-06/2026-06-06T20-05-24-426Z-328008c4fb54917b883d9f98f202985cc11d5b0ce6b4ec6b7650b244b402350a.json |
Event Fields
{
"content_hash": "bfd811784c0f604450f79b00ded27a8b43c7e0976b512a90b9065fd22f6831a4",
"source_hash": "8eb2b3594e290185ca4a494af05bccce8c49bf9a63bc208ffa6882e138bf9a0a",
"last_changed_at": "2026-05-31T17:45:56.288Z",
"active_status": "active"
}Parsed Structured
{
"language": "en",
"location": {
"raw": "Olympus - Sugar Land, TX, Sugar Land, Texas",
"city": "Olympus - Sugar Land",
"region": "TX",
"country": "United States",
"is_remote": false,
"confidence": 0.9
},
"salary_max": 0,
"salary_min": 0,
"inferred_at": "2026-06-06T20:05:25.696Z",
"launch_scope": {
"reason": "english_us_canada",
"included": true,
"language": "en",
"location": {
"raw": "Olympus - Sugar Land, TX, Sugar Land, Texas",
"city": "Olympus - Sugar Land",
"region": "TX",
"country": "United States",
"is_remote": false,
"confidence": 0.9
},
"countries": [
"United States"
]
},
"remote_policy": null,
"salary_period": null,
"workplace_type": "on_site",
"salary_currency": null
}Extensions
{}Native Structured
{
"id": "456820",
"job": {
"id": "467142",
"division": null,
"department": {
"id": "21118",
"name": "Operations "
},
"requisition_id": "PIN-1388",
"structure_custom_group_one": null
},
"url": "https://alcanzaclinical.pinpointhq.com/en/postings/158080b5-9924-4a8b-a41f-a68b8e13efe2",
"path": "/en/postings/158080b5-9924-4a8b-a41f-a68b8e13efe2",
"title": "Clinical Research Physician - Metabolic or Hepatology - part time (16 hours per week)",
"benefits": "<ul><li><!--block-->Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. </li><li><!--block-->Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.</li></ul>",
"location": {
"id": "30853",
"city": "Sugar Land",
"name": "Olympus - Sugar Land, TX",
"province": "Texas",
"postal_code": ""
},
"deadline_at": null,
"description": "<div><!--block-->Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. <br><br>The <strong>Principal Investigator </strong>conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.</div>",
"compensation": null,
"reporting_to": "Alberto Blanco",
"workplace_type": "onsite",
"benefits_header": "Benefits",
"employment_type": "part_time",
"workplace_type_text": "Onsite",
"compensation_maximum": null,
"compensation_minimum": null,
"compensation_visible": false,
"employment_type_text": "Part Time",
"key_responsibilities": "<div><!--block--><strong>Essential Job Duties:</strong></div><ul><li><!--block-->Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes </li><li><!--block-->Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance</li><li><!--block-->Evaluates and assesses participants to ensure only eligible participants enroll into the trials.</li><li><!--block-->Participates and engages in successful delivery and retention of study participants.</li><li><!--block-->Interacts positively and collaboratively with sponsors, clients and team members.</li><li><!--block-->Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.</li><li><!--block-->Actively involved in protocol training for staff.</li><li><!--block-->Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.</li><li><!--block-->Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.</li></ul><div><!--block--><br></div>",
"compensation_currency": null,
"compensation_frequency": null,
"skills_knowledge_expertise": "<div><!--block--><strong>Minimum Qualifications:</strong> MD or DO degree, an active physician license (in good standing) in the state of practice for this role. Clinical research experience is required. Board certification in area of specialty required. CPR required / ACLS preferred.<br><br></div><div><!--block--><strong>Required Skills: </strong></div><ul><li><!--block-->Clinical skills and clinical procedures based on area of specialty. </li><li><!--block-->Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm). </li><li><!--block-->Must possess strong organizational skills, attention to detail, and math proficiency.</li><li><!--block-->Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred.</li><li><!--block-->Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers. </li><li><!--block-->Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.</li><li><!--block-->Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.</li><li><!--block-->Must possess a high degree of urgency, self-motivation, integrity and dependability.</li><li><!--block-->Ability to work independently to identify problems and implement solutions. </li><li><!--block-->Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.</li></ul><div><!--block--><br></div>",
"key_responsibilities_header": "Key Responsibilities",
"skills_knowledge_expertise_header": "Skills, Knowledge and Expertise"
}Get this page with API
Rendered from the bluedoor Job Postings API. Reproduce it:
GET https://api.bluedoor.sh/job-postings/v1/jobs/58f86fac22ca17e13bb643a30caa73ecbeeb5f9a?include=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/82cff78a-f68b-4a7b-9bc0-5a37dd8a10b7JSONGET https://api.bluedoor.sh/job-postings/v1/sources/475d8ecd-9e61-4c5b-8d96-44eb7fb8578bJSONGET https://api.bluedoor.sh/job-postings/v1/jobs/58f86fac22ca17e13bb643a30caa73ecbeeb5f9a/eventsJSON