Anna R.-Clinical Enrollment Manager / Patient Navigator
Check rate
Experience
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.
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.
Freelance CRA
CROs
Senior Clinical Research Associate
IQVIA Biotech
Clinical Team Manager
Ergomed PLC
Clinical Research Department Manager
Bioscience (Neuca group)
Clinical Project Manager
InnoPharma International
Senior Study Management Associate
Allergan LTD
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.
Business area experience
See which departments and functions this freelancer has contributed to most.
Experienced in Research and Development, Operations, Project Management, and 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
Education
Criminal Law Cathedral
Postgraduate, Medical law · Medical law · Kraków, Poland
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
Expertise
Qualifications
Profile
Frequently asked questions
Have questions? Find more information here.
Anna is based in Kraków, Poland.
Anna speaks the following languages: Polish (Native), English (Advanced), French (Advanced), Arabic (Elementary).
Anna has at least 16 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 9 months. Note that Anna may not have shared all experience and actually has more experience.
Based on recent experience, Anna would be well-suited for roles such as: Clinical Enrollment Manager / Patient Navigator, Clinical Trial Liaison, Freelance CRA.
Anna's most recent position is Clinical Enrollment Manager / Patient Navigator at CRO.
In recent years, Anna has worked for CRO, TMac for Geron, CROs, and IQVIA Biotech.
Anna is most experienced in industries like Pharmaceutical, Biotechnology, and Healthcare.
Anna is most experienced in business areas like Research and Development, Operations, and Project Management. Anna also has some experience in Logistics.
Anna has recently worked in industries like Biotechnology, Pharmaceutical, and Healthcare.
Anna has recently worked in business areas like Research and Development, Operations, and Logistics.
Anna holds a Doctorate in Medical law from Criminal Law Cathedral.
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.
The availability of Anna needs to be confirmed.
Daily rate distribution
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Average rates for similar positions
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The average daily rate is the mean of all daily rates from recent contracts of comparable freelancers on our platform.
The median daily rate is the middle value of all daily rates — half of comparable freelancers charge less, half charge more. Unlike the average, it is barely affected by outliers.
Calculated based on our freelancers’ daily rates as of 7 Sep 2026. Actual rates may vary depending on seniority level, experience, skill specialization, project complexity, and engagement length.
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