Medical Scientist
Philadelphia, Pennsylvania, United States · Full Time
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- Experience
- 1–5 yrs
- Salary
- —
- Openings
- 1
- Posted
- منذ 3 ساعات
- Work mode
- In office
- Education
- Bachelor's degree
- Resume
- Required to apply
Where you'll work
Job description
Job Overview
Biofusion in Philadelphia, PA is seeking a Medical Scientist to support various aspects of clinical operations across multiple projects. This role involves managing clinical research activities, ensuring adherence to protocols and regulatory standards, coordinating with cross-functional teams, and overseeing data management for clinical trials.
Key Responsibilities
- Assist clinical project operations by supporting timeline management and deliverable tracking.
- Develop and implement operational strategies for clinical trials.
- Collaborate with external vendors and coordinate daily trial activities.
- Lead and oversee clinical research projects, including developing study protocols and budgets.
- Ensure all clinical activities comply with ethical and regulatory requirements.
- Mentor junior colleagues and manage research teams effectively.
- Coordinate patient recruitment, retention, and communication across study sites.
- Manage data collection processes ensuring accuracy, integrity, and compliance with regulatory standards.
- Prepare analytical reports and maintain thorough documentation for stakeholders and authorities.
Qualifications and Requirements
- Educational background varies according to specialization, including Bachelor's degrees in Health Sciences, Nursing, Life Sciences, or related fields; Master’s or PhD degrees in Clinical Research or Data Science preferred for senior roles.
- Relevant experience ranging from 1 to 5+ years depending on position level, covering clinical operations, research management, clinical trial coordination, data management, or clinical research associate roles.
- Strong organizational, multitasking, leadership, and problem-solving skills.
- Ability to work independently and collaboratively within multidisciplinary teams.
- Familiarity with clinical trial regulations such as GCP, FDA guidelines, and ethical standards.
- Proficiency with clinical data management software and statistical analysis tools is advantageous.
Additional Information
This full-time onsite position in Philadelphia requires professionals capable of managing the complexities of clinical trials from inception to completion. Candidates with strong communication skills and the capacity to work in fast-paced environments will excel. The role may involve mentoring and leading junior staff members to ensure high standards of clinical research integrity and compliance.