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HomeCompaniesAlcanzaclinicalClinical 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

FieldValue
CompanyAlcanzaclinical
TitleClinical Research Physician - Metabolic or Hepatology - part time (16 hours per week)
Normalized title-
Department / teamOperations
LocationOlympus - Sugar Land, TX, United States
Work modelOn Site
Employment typePart Time
Salary0-0
Statusactive
ATS providerPinpoint
Posted / first seen / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Alcanzaclinical.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Pinpoint.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Olympus - Sugar Land.Open
Department jobsActive postings in Operations.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyAlcanzaclinical
Source475d8ecd-9e61-4c5b-8d96-44eb7fb8578b
ATS providerPinpoint

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 ID58f86fac22ca17e13bb643a30caa73ecbeeb5f9a
Org ID82cff78a-f68b-4a7b-9bc0-5a37dd8a10b7
Source ID475d8ecd-9e61-4c5b-8d96-44eb7fb8578b
Board ID475d8ecd-9e61-4c5b-8d96-44eb7fb8578b
Providerpinpoint
Provider Job Key456820
TitleClinical Research Physician - Metabolic or Hepatology - part time (16 hours per week)
Normalized Title
Statusactive
Activeyes
Location TextOlympus - Sugar Land, TX, Sugar Land, Texas
DepartmentOperations
Team
Employment Typepart_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionTX
CityOlympus - Sugar Land
Salary Raw0-0
Salary Min0
Salary Max0
Salary Currency
Salary Period
Source URLhttps://alcanzaclinical.pinpointhq.com/en/postings/158080b5-9924-4a8b-a41f-a68b8e13efe2
Apply URLhttps://alcanzaclinical.pinpointhq.com/en/postings/158080b5-9924-4a8b-a41f-a68b8e13efe2
First Seen At2026-05-31 17:45:56Z
Last Seen At2026-06-06 20:05:25Z
Last Checked At2026-06-06 20:05:25Z
Last Changed At2026-05-31 17:45:56Z
Inactive At
Source Posted At
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=pinpoint/board=alcanzaclinical/date=2026-06-06/2026-06-06T20-05-24-426Z-328008c4fb54917b883d9f98f202985cc11d5b0ce6b4ec6b7650b244b402350a.json
Event Fields
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  "last_changed_at": "2026-05-31T17:45:56.288Z",
  "active_status": "active"
}
Parsed Structured
{
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    "city": "Olympus - Sugar Land",
    "region": "TX",
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    "confidence": 0.9
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Extensions
{}
Native Structured
{
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  "job": {
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    "division": null,
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      "name": "Operations "
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  "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.&nbsp;</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",
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  },
  "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 &amp; HIPAA guidelines, study protocols, as well as company policies and processes&nbsp;</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>&nbsp; MD or DO degree, an active physician license (in good standing) in the state of practice for this role. Clinical research experience is required.&nbsp; Board certification in area of specialty required. CPR required / ACLS preferred.<br><br></div><div><!--block--><strong>Required Skills:&nbsp;</strong></div><ul><li><!--block-->Clinical skills and clinical procedures based on area of specialty.&nbsp;</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).&nbsp;</li><li><!--block-->Must possess strong organizational skills, attention to detail, and math proficiency.</li><li><!--block-->Well-developed written and verbal communication skills.&nbsp; 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. &nbsp;</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.&nbsp;</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"
}
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