Top 6 Principal investigator Jobs in Austin, Tx

Principal Investigator
Pinnacle Clinical Research —Austin, TX
- Weekends as needed
- Spanish
- Medicine
- Vital signs
- Paid holidays
- Disability insurance
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Principal Investigator (MD/DO) – Clinical Research - Austin, TX
The IMA Group —Austin, TX
- Part-time
- Medicine
- BC/BE
- Senior level
- Paid holidays
- Paid time off
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Principal Product Manager, Investigations
SpyCloud —Austin, TX
- $162,000 - $210,000 a year
- Full-time
- Remote
- Computer science
- Computer Science
- 5 years
- Health savings account
- Paid holidays
Principal Investigator
HDR —Austin, TX
- Weekends as needed
- Up to 50% travel
- 5 years
- Office
Cardiometabolic / Endocrinology Principal Inv
Tekton Research Inc —Austin, TX
- Full-time
- Remote
- Medicine
- Travel
- Senior level
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Principal Investigator (MD/DO) – Clinical Research - Austin, TX
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Principal Investigator

Pinnacle Clinical Research -
Austin, TX

Quick Apply

Job Details

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Vision insurance
Life insurance

Qualifications

Delegation

Full Job Description

Summary:

The Clinical Research Physician Investigator or PI is responsible for administering activities to facilitate clinical research and providing clinical support for the conduct and oversight of clinical trials.

The PI agrees to assume the overall responsibility for the study conduct. By doing so, inherently agrees to:

Personally conduct or supervise the research
Ensure that everyone to whom a task is delegated is qualified by virtue of education, training, and experience to perform each of their delegated tasks
Protect the rights, safety, and welfare of the participants who will be under their care. To do this they agree that the research:
- It is conducted in accordance with all federal regulatory requirements, state law, and Pinnacle Clinical Research policies (including SOPs)
- It is conducted in accordance with the IRB-approved plan
- That they will ensure the accuracy, security, and integrity of the research data and the subsequent analysis of that data.

Duties and Responsibilities:

Review and hold expert knowledge of study-related activities and protocols.
Assume all responsibilities and obligations as an Investigator, per Title 21 part 312 and FDA Form 1572.
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times.
Maintain study sponsor and clinical trial confidentiality.
Performs study-related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments. Reviews and adjudicates all lab, imaging, and biopsy findings.
Assists in the preparation of study monitor visits.
Performs subject screening and recruitment.
Provides some weekend coverage to facilitate study visits per protocol.
Provides after-hours phone call coverage as needed.
Oversee Sub-Investigators and recruitment team.

Education/Experience:

One to two years of research experience as a principal investigator is preferred.
At least one to two years of clinical practice in Internal Medicine, Family Practice, Neurology, Geriatrics, Endocrinology, GI +/- liver disease preferred.

Certificates and Licenses:

Current physician license. Board Certified preferred.

Knowledge, Skills, and Other Abilities:

Written and oral communication skills
Bilingual (English and Spanish) strongly preferred
Organizational skills
Ability to pay attention to detail
People skills including possessing a positive, friendly, and professional demeanor
Ability to be flexible with changing priorities
Ability to communicate in a diplomatic and professional manner
Strong interpersonal skills
Strong mathematical knowledge
Excellent computer skills
knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Foxfire, and web-based enterprise solutions software.

Work Environment and Physical demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Work is performed in an office/laboratory and/or a clinical environment.
Exposure to biological fluids and/or bloodborne pathogens.
Personal protective equipment is required such as protective eyewear, garments, and gloves.
Occasional travel may be required domestic and/or international.
Ability to work in an upright and/or stationary position for 6-10 hours per day.
Frequent mobility required.
Occasional squatting, kneeling, or bending.
Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.

Perks of working at Pinnacle Clinical Research:

401k
Medical, dental, vision, long-term disability, short-term disability, FSA, and life insurance
3 weeks of paid time off
13 paid company holidays
CME allowance
Tranquility Room (specific locations apply)
Pinnacle Gym (specific locations apply)
Scrub voucher (specific positions apply)
And more!

Pinnacle Clinical Research is an equal-opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status, or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.

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principal investigator jobs in austin, tx

Principal Investigator

Principal Investigator (MD/DO) – Clinical Research - Austin, TX

Principal Product Manager, Investigations

Principal Investigator

Cardiometabolic / Endocrinology Principal Inv

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