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23 Hours Ago
Frederick, MD, USA
1,114 Employees
61K-65K Annually
Entry level
1,114 Employees
61K-65K Annually
Entry level
Biotech
The Project Controls Engineer supports cross-functional client departments by ensuring alignment during engineering projects, performing due diligence for project deliverables, and proactively troubleshooting issues. They produce key project controls deliverables such as budgets and schedules while contributing to a patient-focused mission through professional development and philanthropic activities.
23 Hours Ago
Raleigh, NC, USA
1,114 Employees
Entry level
1,114 Employees
Entry level
Biotech
Project Farma is a leading consulting firm in advanced therapy technical operations, focusing on biomanufacturing and project management for gene and cell therapy and biotech companies. They aim to advance operational excellence and speed to market for innovative treatments, while fostering a culture of teamwork and professional development.
23 Hours Ago
Raleigh, NC, USA
1,114 Employees
61K-65K Annually
Entry level
1,114 Employees
61K-65K Annually
Entry level
Biotech
The Project Controls Engineer will support cross-functional teams, providing project management and engineering lifecycle assistance. Responsibilities include managing project budgets, schedules, risk assessments, and producing detailed project reports to enhance operational excellence in life sciences.
23 Hours Ago
Bethesda, MD, USA
1,114 Employees
61K-65K Annually
Entry level
1,114 Employees
61K-65K Annually
Entry level
Biotech
As a Project Engineer, you will collaborate with clients in the life sciences sector, providing engineering support and troubleshooting for advanced manufacturing processes. You are responsible for authoring technical documents, executing validation protocols, and fostering cross-functional alignment to ensure project success while embodying a patient-focused mission.
2 Days Ago
Bangalore, Bengaluru, Karnataka, IND
1,114 Employees
Senior level
1,114 Employees
Senior level
Biotech
The Manager Centralized Visit Report Reviewer leads and manages a team focused on ensuring the quality of clinical trial reports. The role involves mentoring, improving operational standards, providing strategic oversight, and ensuring compliance with regulatory requirements while fostering individual career development.
2 Days Ago
Bangalore, Bengaluru, Karnataka, IND
1,114 Employees
Senior level
1,114 Employees
Senior level
Biotech
The Principal Statistical Programmer is responsible for performing all SAS programming tasks for clinical trial analysis and reporting. Responsibilities include collaborating across departments, developing and validating SAS programs for statistical analysis, creating randomization lists, and leading internal projects. The role also involves training, advising on programming techniques, and ensuring compliance with regulatory requirements.
3 Days Ago
Bangalore, Bengaluru, Karnataka, IND
1,114 Employees
Senior level
1,114 Employees
Senior level
Biotech
The Lead Data Engineer oversees a team of data engineers in ensuring the implementation and maintenance of data standards for Precision for Medicine’s laboratory services. Responsibilities include leading projects, developing biomarker data management code, executing data processing pipelines, and collaborating with various stakeholders to guarantee high-quality data delivery.
3 Days Ago
United States
Remote
1,114 Employees
97K-145K Annually
Senior level
1,114 Employees
97K-145K Annually
Senior level
Biotech
The Feasibility Manager in the Precision for Medicine team oversees the management and delivery of various feasibility projects related to clinical trials. They conduct pre-award and post-award analyses, support business development efforts, and ensure the quality and accuracy of feasibility data and processes throughout the project lifecycle. The role involves collaboration with operational strategy teams and client interactions to support successful trial execution.
4 Days Ago
India
Remote
1,114 Employees
Mid level
1,114 Employees
Mid level
Biotech
The Sr SAS Programmer at Precision for Medicine will develop and maintain SAS programming to support clinical data review, creating outputs like metrics and reconciliation reports. Responsibilities include validating SAS programs, ensuring timely project delivery, troubleshooting issues, participating in training, and contributing to SOPs. This role focuses on non-standard statistical programming related to clinical trials.
5 Days Ago
United States
Remote
1,114 Employees
108K-162K Annually
Mid level
1,114 Employees
108K-162K Annually
Mid level
Biotech
The Study Enrollment Lead coordinates and optimizes site recruitment strategies for clinical trials, supporting Clinical Research Associates (CRAs) through training and coaching. Responsibilities include developing site recruitment plans, ensuring effective communication with site staff, and collaborating with various teams to align recruitment efforts with study goals.
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