Top 4 Senior collection associate pharmacy Jobs in Mount Laurel, Nj

Senior In-House Clinical Research Associate
Cabaletta Bio —Philadelphia, PA
- Nursing
- Mid-level
- Master's degree
- Health insurance
- Paid time off
1d
Senior Collection Associate - Pharmacy
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- Full-time
- Computer literacy
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PharMerica —Philadelphia, PA
- Full-time
- Writing skills
- Mid-level
- 3 years
- Disability insurance
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Senior Regulatory Affairs Specialist
Iovance Biotherapeutics —Philadelphia, PA
- $140,000 - $160,000 a year
- Microsoft Excel
- Bachelor of Science
- Master's degree
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Senior Collection Associate - Pharmacy
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Assigned duties include researching account balances and following up with collection calls to insurers and parents. Reviewing claims with no response.
$28.05 - $35.05 an hour
Quick Apply
Senior In-House Clinical Research Associate
Cabaletta Bio —Philadelphia, PA
A bachelor's or master's degree in a relevant field, such as life sciences, nursing, or pharmacy. The Senior In-House Clinical Research Associate (CRA) supports…
1d

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Senior In-House Clinical Research Associate

Cabaletta Bio
Philadelphia, PA

Apply Now

Job Details

1 day ago

Benefits

Stock options
Health insurance
Paid time off

Qualifications

Research project management
Vendor selection
Clinical audit and monitoring
ICH guidelines
Vendor compliance management
Clinical program monitoring
Vendor relationship management
Vendor communication
Relationship management
Productivity software
Clinical quality assurance standards
Clinical trial site selection
Cross-functional communication
FDA regulations

Full Job Description

About the Position

The Senior In-House Clinical Research Associate (CRA) supports the planning, execution, and oversight of Cabaletta Bio’s clinical trials, serving as a key operational and external-facing partner to clinical sites, CROs, and other vendors. This role works cross-functionally with Clinical Project Management and the broader Clinical Operations team to ensure high-quality trial conduct, strong site and vendor relationships, and inspection-ready documentation throughout the study lifecycle. This role will play a key part in bringing complex studies forward in a fast-paced, mission-driven environment. This role will report to the Senior Clinical Trial Manager/Associate Director Clinical Operations.

Responsibilities Include

Provide monitoring oversight by reviewing monitoring reports and escalating any trends related to data quality or study conduct to the appropriate CTM, Clinical Operations.
Support the oversight of activities of CRO and study vendors to ensure compliance with the study protocol and on-time achievement of overall clinical objectives and deliverables.
Contribute to the development of study documentation including protocol review, creating study manuals, ICFs, study plans and CRFs.
Contribute to and partner with the CRO for study start-up activities including site feasibility and selection.
Support the Clinical Operations team and cross-functional representatives as required in relationship management tasks (e.g., study logistics, patient enrollment, safety, data management, etc.) to accurately coordinate clinical study activities.
Ensure that study documentation is maintained according to applicable regulations, industry accepted standards, and SOPs that govern clinical studies.
Collaborate with Clinical, Regulatory, Quality, and other cross functional team members to ensure compliance and inspection readiness.
Identify and resolve study-related issues and deviations, as needed.
Communicate with study sites and investigators.
Provide support to study sites, including training and troubleshooting.
Support various administrative tasks for the Clinical Operations team including scheduling meetings and taking minutes.
Perform clinical research site activities, such as onsite or remote co-monitoring, training, motivational, and sponsor oversight visits, as needed.
Perform other duties and assignments as required for the overall success of the projects.

Required Qualifications

A bachelor's or master's degree in a relevant field, such as life sciences, nursing, or pharmacy.
At least 2-3 years of experience in clinical research, preferably in a CRA or related role.
Experience with all aspects of trial and site startup and vendor selection and management, study management, monitoring and study close-out.
Strong knowledge of clinical trial conduct, GCP, FDA regulations, and ICH guidelines.
Excellent written and verbal communication skills to effectively communicate with study sites, investigators, and internal study team members.
Strong organizational skills to manage multiple tasks and priorities simultaneously.
Strong attention to detail to ensure accurate and complete data collection and documentation.
Proficiency in Microsoft Office applications and experience working with electronic data capture systems (EDC).
Ability to build positive relationships with study sites and investigators.
Flexibility to adapt to changing project needs and timelines.
Strong team orientation and passion for continuous self-development.
Experience in a startup setting is preferred.
Ability to travel up to 10%, if needed.

How to Apply

Please click the link at the bottom of the posting to submit an application.

Benefits

Our most important asset is our people and we offer competitive benefits including health and retirement, PTO, and stock option plans.

Equal Opportunity Employer

Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law.

Apply Now

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senior collection associate pharmacy jobs in mount laurel, nj

Senior In-House Clinical Research Associate

Senior Collection Associate - Pharmacy

Client Success Manager / Sr Living / Long-Term Care Pharmacy

Senior Regulatory Affairs Specialist

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