Anna Rosowicz-Lipowczan - Clinical Enrollment Manager / Patient Navigator

Q: Where is Anna based?

Anna is based in Kraków, Poland .

Q: What languages does Anna speak?

Anna speaks the following languages: Polish (Native), English (Advanced), French (Advanced), Arabic (Elementary) .

Q: How many years of experience does Anna have?

Anna has at least 15 years of experience. During this time, Anna has worked in at least 9 different roles and for 9 different companies . The average length of individual experience is 2 years and 8 months . Note that Anna may not have shared all experience and actually has more experience.

Q: What is Anna's latest experience?

Anna's most recent position is Clinical Enrollment Manager / Patient Navigator at CRO .

Q: What companies has Anna worked for in recent years?

In recent years, Anna has worked for CRO , TMac for Geron , CROs , and IQVIA Biotech .

Q: Which industries is Anna most experienced in?

Anna is most experienced in industries like Pharmaceutical , Biotechnology , and Healthcare .

Q: Which business areas is Anna most experienced in?

Anna is most experienced in business areas like Research and Development , Operations , and Project Management . Anna also has some experience in Logistics .

Q: Which industries has Anna worked in recently?

Anna has recently worked in industries like Biotechnology , Pharmaceutical , and Healthcare .

Q: Which business areas has Anna worked in recently?

Anna has recently worked in business areas like Research and Development , Operations , and Logistics .

Recommended expert

Kraków, Poland

Experience

Jan 2025 - Present

1 year 3 months

Clinical Enrollment Manager / Patient Navigator

CRO

Perform site optimisation services to boost patient recruitment for clients' clinical trials.
Conduct market area research prior to in-person visits to assist in logistical preparation.
Engage in community outreach visits at sites or predefined healthcare and patient-focused environments within the site's catchment area to increase awareness of clinical trials among HCP and non-HCP stakeholders.
Provide necessary information and engage in discussion with predefined stakeholders to support patient recruitment.

Jan 2021 - Dec 2023

3 years

Clinical Trial Liaison

TMac for Geron

Engage site staff and investigators in discussion to understand and report challenges in subject enrollment and retention and offer potential solutions.
Assist in the implementation and oversee the execution of site-based patient recruitment tactics.
Communicate investigator/study coordinator inquiries requiring follow-up to designated contacts within Geron and/or the Clinical Research team.
Interpret and report findings with recommendations for action to relevant stakeholders.
Work toward meeting established program metrics.
Upon request, educate clinical trial sites and referring physicians about clinical trial protocol, disease state or study design.
As assigned, attend local, regional and national medical conferences, to obtain new competitive information, stay informed of clinical trends and support and maintain relationships with key investigators.
Complete all administrative responsibilities consistent with SOPs and departmental guidelines including required training, field activity documentation, expense reporting and other assigned tasks.
Participate in and successfully complete all internal education and training on SOPs, policies and relevant products, as well as all compliance training and regulatory education relevant to the pharmaceutical industry.
Interact and build positive relationships with key stakeholders on the Clinical Research team such as the site's assigned study team members including field monitors, CRAs, CTMs and appropriate Geron and CRO staff.
Coordinate all site facing activities with the appropriate study team members from Geron and CRO.
Proactively communicate plans, findings and insights to TMAC, CRO and Geron staff.
Communicate any adverse event information, reports of concern or product complaints in accordance with Geron's policies.
Document all interactions and submit executed documents promptly.
Schedule travel and submit travel expenses within Geron and TMAC travel policies.

Jan 2021 - Dec 2021

1 year

Freelance CRA

CROs

Jan 2018 - Dec 2021

4 years

Senior Clinical Research Associate

IQVIA Biotech

Jan 2017 - Dec 2018

2 years

Clinical Team Manager

Ergomed PLC

Jan 2016 - Dec 2017

2 years

Clinical Research Department Manager

Bioscience (Neuca group)

Jan 2015 - Dec 2016

2 years

Clinical Project Manager

InnoPharma International

Jan 2014 - Dec 2014

1 year

Senior Study Management Associate

Allergan LTD

Jan 2010 - Dec 2015

6 years

Clinical Research Associate

CROs (KCR, INC, RPS)

Industry Experience

See where this freelancer has spent most of their professional time.

Experienced in Pharmaceutical, Biotechnology, and Healthcare.

Pharmaceutical

Biotechnology

Healthcare

Business Area Experience

See which departments and functions this freelancer has contributed to most.

Experienced in Research and Development, Operations, Project Management, and Logistics.

Research and Development

Operations

Project Management

Logistics

Summary

Experienced Senior Clinical Research Associate with a demonstrated history of working in the pharmaceutical industry. Skilled in Electronic Data Capture (EDC), SDV, Translation, Oncology, and Feasibility Studies. Strong research professional with a postgraduate focused in Medical Law from Criminal Law Cathedral, Jagiellonian University. Member of GCP Association. Focused on results.

Skills

Driving License

Languages

Polish

Native

English

Advanced

French

Advanced

Arabic

Elementary

Education

Oct 2012 - Jun 2013

Criminal Law Cathedral

Postgraduate, Medical law · Medical law · Kraków, Poland

Oct 2002 - Jun 2007

Collegium Medicum of Jagiellonian University

Public Health · Kraków, Poland

Certifications & licenses

AI Certificate

KCBSI

Minimum Criteria For ICG E6 (R2) GCP

Nida Training

Transportation Of Dangerous Goods TDG / IATA Course Group 1

Citi Program

Statistics

Experience

Total positions 9

Experience in Pharmaceutical 13 y

Avg length 2 y 5 m

Longest experience 5 y 11 m

Expertise

Recent roles Clinical Enrollment Manager / Patient Navigator, Clinical Trial Liaison, Freelance CRA

Main industries Pharmaceutical, Biotechnology, Healthcare

Main business areas Research and Development, Operations, Project Management

Qualifications

Highest degree Doctorate

Certifications earned 3

Profile

Created

October 2025

Need a freelancer? Find your match in seconds.

Try FRATCH GPT

Frequently asked questions

Do you have questions? Here you can find further information.

Where is Anna based?

Anna is based in Kraków, Poland.

What languages does Anna speak?

Anna speaks the following languages: Polish (Native), English (Advanced), French (Advanced), Arabic (Elementary).

How many years of experience does Anna have?

Anna has at least 15 years of experience. During this time, Anna has worked in at least 9 different roles and for 9 different companies. The average length of individual experience is 2 years and 8 months. Note that Anna may not have shared all experience and actually has more experience.

What roles would Anna be best suited for?

Based on recent experience, Anna would be well-suited for roles such as: Clinical Enrollment Manager / Patient Navigator, Clinical Trial Liaison, Freelance CRA.

What is Anna's latest experience?

Anna's most recent position is Clinical Enrollment Manager / Patient Navigator at CRO.

What companies has Anna worked for in recent years?

In recent years, Anna has worked for CRO, TMac for Geron, CROs, and IQVIA Biotech.

Which industries is Anna most experienced in?

Anna is most experienced in industries like Pharmaceutical, Biotechnology, and Healthcare.

Which business areas is Anna most experienced in?

Anna is most experienced in business areas like Research and Development, Operations, and Project Management. Anna also has some experience in Logistics.

Which industries has Anna worked in recently?

Anna has recently worked in industries like Biotechnology, Pharmaceutical, and Healthcare.

Which business areas has Anna worked in recently?

Anna has recently worked in business areas like Research and Development, Operations, and Logistics.

What is Anna's education?

Anna holds a Doctorate in Medical law from Criminal Law Cathedral.

Does Anna have any certificates?

Anna has 3 certificates. These include: AI Certificate, Minimum Criteria For ICG E6 (R2) GCP, and Transportation Of Dangerous Goods TDG / IATA Course Group 1.

What is the availability of Anna?

Anna is immediately available for suitable projects.

What is the rate of Anna?

Anna's rate depends on the specific project requirements. Please use the Meet button on the profile to schedule a meeting and discuss the details.