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CLIA Laboratory Director (high-complexity) AP/CP Pathologist

Location:
Milton, MA
Posted:
May 04, 2023

Contact this candidate

Resume:

Angela Aimee Steinhardt

**** **** **** ***

Milton, MA 02186

Telephone: 765-***-****

E-Mail: adwxac@r.postjobfree.com

Licensure and

Certification

Louisiana Board of Medicine

Medicine and Surgery License Number: 331162

Issue Date: 5/24/2022; Expiration Date: 5/31/2024; Current Status: Active

LA Controlled Substance License Number: CDS.064014-MD Issued: 10/07/2022

Expiration Date: 10/07/2023

Current Status: Active

DC Board of Medicine

Medicine and Surgery License Number: MD210002104 Issue Date: 03/08/2022; Expiration Date: 12/31/2024

DC Controlled Substance License Number: CS210126331 Expiration Date: 12/31/2024

Current Status: Active

Massachusetts Board of Registration in Medicine

Medical License, Number: 242648

Issue Date: 05/19/2010

Expiration Date: 05/30/2025

Current Status: Active

Massachusetts Controlled Substance Registration Number: MS0908256A Issue Date: 04/04/2013

Expiration Date: 06/02/2025

Address of Registration: 85 West St, Walpole, MA 02081-1844 DEA Registration Number: FS3789647; XS3789647

Schedules: 2, 2N, 3, 3N, 4, 5

Business Activity: Practitioner-DW/275

Issue Date: 02/13/2019

Expiration Date: 02/28/2025

Address of Registration: 85 West St, Walpole, MA 02081-1844 Education and

Training

Medical Board of California

Medical License, Number: A112942

Issue Date: June 25, 2010

Expiration Date: May 31, 2024

Current Status: Active

Indiana Board of Pharmacy

Pharmacist License, Number: 26020928A

Issue Date: 08/14/2002

Expiration Date: 06/30/2024

Current Status: Active

Suboxone Certification, American Academy of Addiction Psychiatry Office Based Buprenorphine Treatment

June 6, 2013

American Board of Pathology

Board Certified in AP/CP Pathology

Examination Date: 05/22/2017

American Board of Pathology Diplomate, 8/7/2017

American Red Cross

Adult/Child/Infant CPR/First Aid/AED Online

Issued: 04/05/2023

Expires: 04/05/2025

Massachusetts Cannabis Control Commission

Medical Use of Marijuana Online System

Registered Medical Provider

Registration Number: D16821

Start Date: 03/16/21

Purdue University School of Pharmacy

West Lafayette, IN 47907

Bachelor of Science: May 11, 2002

Graduation with Distinction (Top 10% of Class)

Cumulative GPA: 3.74/4.00

Class Rank: 5/60

August 2003—June 2007

Indiana University School of Medicine

Indiana University-Purdue University-Indianapolis Medical Center Indianapolis, IN 46202

Doctor of Medicine: June 30, 2007

July 2007-June 2008

Pathology GI Cancer Research Fellowship

Johns Hopkins University School of Medicine

Department of Gastrointestinal Pathology

1550 Orleans St, CRB2-316

Baltimore, MD 21287

July 1, 2008-June 30, 2010

AP/CP Pathology Residency

David Geffen School of Medicine @ UCLA

UCLA Medical Center

10833 Le Conte Ave

Los Angeles, CA 90095

July 1, 2010-June 30, 2012

AP/CP Pathology Residency

Harvard Medical School

Beth Israel Deaconess Medical Center

330 Brookline Ave

Boston, MA 02115

July 1, 2012-June 30, 2013

General Surgical Pathology Fellowship

Subspecialty Focus: Genitourinary Pathology

Harvard Medical School

Beth Israel Deaconess Medical Center

330 Brookline Ave

Boston, MA 02115

Harvard University Extension School

Cambridge, MA

Masters of Liberal Arts, Finance

Graduation Date: May 26, 2016

Recent

Work Experience

April 22, 2021-Present

May 2021-Present

Assurance Scientific

2 Perimeter Park South

Birmingham, AL 35243

205-***-****

Laboratory Director Consultant (High Complexity)

I oversee operations in laboratories offering wound culture molecular PCR testing for podiatrist offices. I review QA/QC and validation studies, perform corrective action if needed, do proficiency testing, and prepare for inspections.

Leafwell MD

04/09/2021-Present

Medical Cannabis Certification Consultant

HIPAALINE LLC

9100 S DADELAND BLVD STE 1701

MIAMI FL 33156

Perform patient histories to determine if patients qualify for therapeutic cannabis in the state of Massachusetts, California, Louisiana and Washington DC.

March 12, 2021-December 2, 2022

DTPM

913 Airport Road W.

Fort Payne, AL 35968

Laboratory Director and Technical Supervisor (High Complexity) P: 256-***-****, ext 245

Oversee operations in a laboratory which does urine toxicology testing. I sign off on QA/QC studies, validation studies, review temperature charts, review proficiency testing results and prepare for inspections. October 26, 2020-June 16, 2023

Octapharma Plasma

752 Crescent St

Brockton, MA 02302

Licensed Physician Consultant

I review medical charts and donor reaction reports and help to train physician substitutes to do patient histories and physical exams. Review SOPs for changes and do competency assessments for technicians and physician substitutes. Center closed on May 19, 2023.

August 27, 2019-September 30, 2020

Thrive Earlier Detection Corp

138 Sidney St

Cambridge, MA 02139

Laboratory Director (High Complexity)

Oversee operations in a laboratory which does genetic testing for cancer biomarkers. I sign off on QA/QC studies, validation studies, review proficiency testing results and prepare for inspections. April 26, 2019-June 30, 2022; March 1, 2023-Present Commonwealth Diagnostics International, Inc

39 Norman St

Salem, MA 01970

Laboratory Director and Technical Supervisor (Moderate Complexity) Oversee operations in a laboratory which does IBSChek testing for Gastrointestinal (GI) bacterial overgrowth in patients with GI complaints. I sign off on QA/QC studies, validation studies, review proficiency testing results and prepare for inspections.

August 10,2017- Present

Path AI

120 Brookline Ave

Boston, MA 02215

Consultant Digital AI Research Pathologist

I’m a digital pathologist who reviews slides to correct heatmaps that differentiate tumor, stroma and normal areas of a tissue. I also perform corrections on heatmaps that differentiate different cell types (lymphocytes, cancer cells, stromal cells, fibroblasts, macrophages, plasma cells, endothelial cells). The work I do leads to the improvement of machine learning technology used to assist pathologists doing diagnostic and research work.

April 4, 2016—December 31, 2020

Aspenti Health

57 Commerce Way

Woburn, MA 01801

Laboratory Director (High complexity)

Oversee operations in a laboratory which does urine toxicology testing. I sign off on QA/QC studies, validation studies, review temperature charts, review proficiency testing results and prepare for inspections. November 11, 2013—July 31, 2019

Discovery Diagnostic Labs

186 Cedar Hill St

Marlborough, MA 01752

Laboratory Director (High Complexity)

Oversee operations in a laboratory which does urine toxicology testing. I sign off on QA/QC studies, validation studies, review temperature charts, review proficiency testing results and prepare for inspections. July 1, 2016--present

Anchor Medical and Wellness Group

85 West St

Walpole, MA 02081

508-***-****

Suboxone/Addiction Medicine Physician

This position involves the evaluation and treatment of patients with opioid dependence with Suboxone. I review their lab results and discuss them with every patient at each visit and provide medication counseling. If patients are struggling, I will try to get them treatment through an inpatient detox program or an intensive outpatient treatment program.

July 1, 2013—June 30, 2016

Bay State Medical Associates, PC

1717 Main St

Brockton, MA 02301

508-***-****

Suboxone Medication Counseling Physician

This position involves the evaluation and treatment of patients with opioid dependence with Suboxone. I review their lab results and discuss them with every patient at each visit and provide medication counseling. If patients are struggling, I will try to get them treatment through an inpatient detox program or an intensive outpatient treatment program.

July 30, 2013—March 1, 2014

Quest Diagnostics

3 Sterling Dr

Wallingford, CT 06492

203-***-****

Staff Pathologist (Monday-Friday)

I practiced as a general surgical pathologist reviewing histopathology and cytopathology cases from multiple tissue types (GYN, GI, GU, skin, blood smears, lung, thyroid). I communicated results to other physicians as well as prepare reports that describe the findings of biopsies and surgical resections. Oct 1, 2013—March 1, 2014

Quest Diagnostics

7 Germantown Rd

Danbury, CT 06810

203-***-****

Lab Director

Oct 1, 2013—March 1, 2014

Quest Diagnostics

2 Church St S Ste 115

New Haven, CT 06519

203-***-****

Lab Director

Oct 1, 2013—March 1, 2014

Quest Diagnostics

1008 N. Main St

Branford, CT 06405

203-***-****

Lab Director

At Quest, I also overseed the operations of 3 different laboratories that performed mainly hematology and chemistry testing. I sign off on QA/QC studies, validation studies, review temperature charts, review proficiency testing results and prepare for inspections.

Awards and Honors

2019 Top Doctor Award (AP/CP Pathology and Addiction Medicine) 2002 The National Dean’s List 25th Edition (2001-2002) 2002 The Honor Society of Phi Kappa Phi

2001 Omicron Delta Kappa National Leadership Society

• Secretary (2001-2002)

● Vice-President for Membership (2002)

2001 Purdue University Homecoming Queen Finalist

2001 The Rho Chi Society

2001 Joseph E. McSoley Pharmacy Scholarship Recipient 2001 National Scholars Honor Society

2001 Iota Sigma Pi National Chemistry Honor Society 2001 Psi Chi National Honor Society in Psychology

2001 National Society of Collegiate Scholars

2001 Beta Beta Beta National Biological Honor Society 2001 Alpha Epsilon Delta Pre-Medical Honor Society

• Co-Treasurer, Physician Shadowing Coordinator (2001) 2001 Alpha Sigma Lambda National Honor Society

• Vice-President (2001-2002)

2000 Helen Carney Scholarship Recipient

1998 Golden Key National Honor Society

1998 Phi Lambda Sigma Pharmacy Leadership Society

1996 Alpha Lambda Delta Freshman Honorary

1996 Phi Eta Sigma Freshman Honorary

1995-2002 Dean’s List

1995-2002 Semester Honors

Volunteer

Experience

Research

Experience

2005 Impact Christian Health Center Medical Student Volunteer 2001 The Rho Chi Society—March of Dimes Walk America 2001 Alpha Epsilon Delta--Lafayette Urban Ministry Volunteer 1999 Phi Lambda Sigma Ronald Mc Donald House Project 1998 Phi Lambda Sigma Community Recycling Project

1997 Kappa Epsilon Breast Cancer Awareness Project 1996 Alpha Lambda Delta—Soup Kitchen Volunteer

1996 American Red Cross Disaster Services Course 1995 Special Olympics Volunteer

May 2004—August 2004

Center for Paralysis Research

Purdue University

West Lafayette, IN 47907

Faculty Mentor: Richard Borgens,PhD

Project Title: Axonal sealing time in crush injuries vs. transaction injuries of the spinal cord

Brief Description: I placed 2 sections of guinea pig spinal cords with newly induced injuries—one section with transection injury and one section with crush injury in an isotonic solution with Fluoro-Ruby® dye for about 60 minutes. Then, I froze the sections with liquid nitrogen and made thin frozen sections (5 micrometer thick). From these sections, I could determine the distance the dye migrated through the axon (before the axon seals off) by counting the number of sections which contained the fluorescent dye. Examination of the sections containing the fluorescent dye was identified using a fluorescent microscope. Then, I divided the distance (# of thin sections containing dye x 5 micrometers/thin section) by duration of injury

(60 minutes) to get the axonal sealing time. Then, I compared the results for crush injuries vs. transaction injuries.

July 2007—June 2008

Department of Pathology

Johns Hopkins University School of Medicine

Baltimore, MD 21287

Faculty Mentor: Robert A. Anders, MD, PhD

Project 1 Title: Expression of Yes Associated Protein in Common Solid Tumors

In this study, YAP expression intensity in normal vs. neoplastic tissues of the colon, lung, ovary, and breast was investigated. Using patient tissue biopsies prepared into tissue microarrays and immunohistochemistry methods, YAP expression level was determined using a scoring system to measure intensity as negative, low, or high. Based on the results of the experiment, we concluded that YAP expression intensity is higher in neoplastic tissues than in normal tissues suggesting that a common oncogenic pathway involving YAP maybe involved in the process of tumorigenesis in different tissue types.

Project 2 Title: Investigation of a Novel Oncogenic Pathway in Hepatocellular Carcinoma

In this study, I investigate the amplification of the YAP gene in the genomic DNA of human hepatocellular carcinoma by using RT-PCR methods. YAP immunohistochemistry was used to compare YAP expression in normal liver cells vs. neoplastic cells of hepatocellular carcinoma. Results of experiments performed to date demonstrate amplification of YAP in the hepatocellular carcinoma cell lines vs. normal liver cells.

July 2009—August 2012

Department of Pathology

UCLA School of Medicine

Los Angeles, CA 90095

Faculty Mentor: Jonathan Braun, MD/PhD

Project Title: Progesterone Receptors A and B in Grade 1 Endometrial Adenocarcinoma and Complex Atypical Hyperplasia Predict Response to Progestin Therapy

Abstract for College of American Pathologists (CAP) Meeting 2010: Progesterone Receptors A and B in Grade 1 Endometrial Adenocarcinoma and Complex Atypical Hyperplasia Predict Response to Progestin Therapy Kristine Penner, MD, MPH1, Madhuri Wadehra, PhD2, Angela Steinhardt, MD, Claire Hogue2, Jonathan Braun, MD, PhD2, and Oliver Dorigo, MD, PhD1 1Departments of Obstetrics and Gynecology and, UCLA Medical Center, Los Angeles, California

2Departments of Pathology, UCLA Medical Center, Los Angeles, California Context: Ten percent of grade 1 endometrial adenocarcinomas (G1EACs) and complex atypical hyperplasias (CAHs) occur in patients younger than age 40. Progestin therapy is an option to preserve fertility, but no biologic markers that predict response are known. We investigated whether progesterone receptor isoforms A

(PRA) and B (PRB) at initial endometrial biopsy or first follow-up biopsy post- progestin therapy might predict treatment response. Design: We retrospectively identified premenopausal patients with CAH or G1EAC who had undergone progestin therapy for more than 8 weeks and for whom there was outcome data and available specimens pretreatment and within the first 9 months post-treatment. Immunohistochemical staining for PRA and PRB was performed on all tissues, tumors, and stroma. Results were evaluated using a histologic scoring system.

Results: We identified 38 subjects (median age, 36 years; age range, 23 to 48 years) who had an initial pathology of G1EAC (35%) or CAH (65%). Of these subjects, 50% had documented resolution to normal histopathology (median time, 7 months). Levels of both PRA and PRB were greater pretreatment versus post-treatment (P < .05); pretreatment expression of both isoforms was greater in tumor versus stroma (P <

.01); at first follow-up, there was no difference in expression between tumor tissue and stroma for either isoform; and a higher proportion of PRA (>0.6) to total PR in the initial specimen correlated with a higher likelihood of disease resolution (P = .04). Conclusions: The ratio of PRA and PRB for young patients with CAH or G1EAC at initial diagnostic biopsy may be a useful guide to individual likelihood of resolution of G1EAC or CAH with progestin therapy.

Abstract for United States and Canadian Academy of Pathology

(USCAP) Meeting 2011:

Progesterone Receptors A and B, pAkt, and p4EBP1 Expression Patterns in Grade 1 Endometrial Adenocarcinoma(G1EAC) and Complex Atypical Hyperplasia(CAH) and Prediction of Response to Progestin Therapy

Kristine Penner, Madhuri Wadehra, Angela Steinhardt, Claire Hogue, Ilana Cass, Christine Walsh, Christine Holschneider, Jonathan Braun and Oliver Dorigo 1Department of Obstetrics and Gynecology and Department of Pathology, UCLA Medical Center, Los Angeles, CA, United States; 2Olive View-UCLA Medical Center, Los Angeles, CA, United States and 3Cedars Sinai Medical Center, Los Angeles, CA, United States.

Background: Progestin therapy is a treatment option for CAH and G1EAC in women who desire fertility preservation. No markers that reliably predict response to treatment have been identified. Progesterone receptor status and activation of the pAkt/PTEN pathway have each been hypothesized to influence the effectiveness of progestin treatment. Progesterone receptor B(PRB)activation is known to alter the activity of this pathway. We investigated whether expression of progesterone receptor A(PRA) and B(PRB) as well as markers in the pAkt/PTEN pathway (pAkt and p4EBP1) change in response to progestin therapy and if any of these markers could be used to predict therapeutic response.

Design: Premenopausal patients with CAH or G1EAC who underwent progestin therapy for at least 8 weeks between 1998-2007 were retrospectively identified from three institutions. Patients had an initial diagnostic endometrial biopsy and a follow-up biopsy during the first nine months of treatment. Immunohistochemical (IHC) staining for PRA, PRB, pAkt and p4EBP1 was performed on all tissue. The H score system was used by a pathologist to quantify the IHC staining. H score>50 is considered positive with 50-100 weakly positive, 100-200 moderately positive, and 200-300 strongly positive. Tumor tissue was scored separately from stroma. Results: 38 subjects were identified with a median age of 36 years (range 23- 48).Moderate staining (H score >100) for PRA, PRB and pAkt was seen in 79%, 84%,and 62% of initial biopsies, respectively. Expression levels of all markers (PRA, PRB, pAkt, p4EBP1) were greater in the initial biopsy than after treatment

(p<0.05).Strong(H score >200) expression of PRB in the initial biopsy was significantly associated with resolution(83% vs. 44% resolution, p=.035). Laboratory Skills

Research

Publications and

Poster

Presentations

Organization/Club

Memberships

Conclusions: Our data suggests that progestin therapy appears to reduce expression of PRA, PRB, pAkt, and p4EBP1 in CAH and G1EAC, and hence, may influence activation of the pAkt/PTEN pathway. Strong PRB expression in both the initial and first follow-up biopsies with CAH or Grade 1 EA has the potential to predict response to progestin treatment. Staining for PRB in a patient's initial diagnostic biopsy therefore may provide additional information to assist in counseling patients regarding their individual likelihood of resolution of G1EAC and CAH with progestin therapy.

Preparing and splitting cell cultures, performing RT-PCR, pipetting, electrophoresis, immunohistochemistry staining techniques, handling laboratory mice, maintaining a laboratory journal, scientific writing Steinhardt AA, Gayyed MF, Klein AP, Dong J, Maitra A, Pan D, Montgomery EA, Anders RA. Expression of the Yes Associated Protein in Common Solid Tumors. Human Pathology. 39 (11):1582-1589.

Penner K, Wadehra M, Holschneider C, Cass I, Walsh I, Steinhardt A, Hogue C, Braun J, Dorigo O. Progesterone Receptor A and B Expression in Grade 1 Endometrial Adenocarcinoma and Complex Atypical Hyperplasia Predicts Response to Progestin Therapy. Oral Plenary Presentation: 39th annual meeting of the Western Association of Gynecologic Oncologists, Santa Barbara, CA, June 2010.

Penner K, Wadhuri M, Steinhardt A, Hogue C, Braun J, Dorigo O. Progesterone Receptors A and B in Grade 1 Endometrial Adenocarcinoma and Complex Atypical Hyperplasia Predict Response to Progestin Therapy.

(2010) Abstracts and Case Studies From the College of American Pathologists 2010 Annual Meeting. Archives of Pathology & Laboratory Medicine: Vol. 134, No. 9, pp. 1283-1396, September 2010. Penner K, Wadhuri M, Steinhardt A, Hogue C, Cass I, Walsh C, Holschneider C, Braun J, Dorigo O. Progesterone Receptors A and B, pAkt, and p4EBP1 Expression Patterns in Grade 1 Endometrial Adenocarcinoma(G1EAC) and Complex Atypical Hyperplasia(CAH) and Prediction of Response to Progestin Therapy (2011). United States and Canadian Academy of Pathology 2011 Annual Meeting. Laboratory Investigation 91, 263A, February 2011.

Penner K, Wadehra M, Steinhardt A, Hogue C, Cass I, Holschneider C, Walsh I, Braun J, Dorigo O. Expression of progesterone receptor and p4EBP1 as molecular predictors of response to progestin treatment in endometrial adenocarcinoma and complex atypical hyperplasia. Poster Presentation: 102nd annual meeting of the American Association for Cancer Research, Orlando, FL, April 2011.

Petrie M, Lynch K, Wu A, Steinhardt A, Horowitz G. Prescription Compliance or Illicit Designer Drug Abuse? Clinical Chemistry 58:12-201*-****-**** Harvard Kendo Club

2011-2016 Harvard Ballroom Dance Team

2011-2016 Harvard Extension Business Society

2010-present Harvard Club of Boston

2010-present College of American Pathologists (CAP) 2010-present Massachusetts Medical Society

2009-present United States and Canadian Academy of Pathology 2008-2010 Los Angeles Society of Pathologists

2003-2007 American Medical Student Association

2003-present Purdue University Alumni Association

2003-2007 American College of Physicians—

American Society of Internal Medicine

2003-present American Medical Association

2002-2003 Indiana Pharmacists Alliance

2001-2002 Caduceus Club for Pre-Medical Students

1999 Psychology Club--Crisis Center Volunteer

1997-2000 Kappa Epsilon Pharmaceutical Sorority

References

Amy Pearsall, MD

Medical Director, Anchor Medical and Wellness Group 85 West St

Walpole, MA 02081-1844

Phone: 646-***-****

Debra Leary

Operational Manager/Lab Supervisor

Anchor Medical and Wellness Group

85 West St

Walpole, MA 02081-1844

508-***-****

Deborah Sumner

President at Quality Systems and Compliance

100 Cummings Center

Suite 233C

Beverly, Massachusetts, USA 01915

978-***-****

508-***-****



Contact this candidate