Sr. Clinical Research Coordinator

Myana; Philadelphia (Philadelphia County); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Comprehensive medical insurance

Tuition assistance

Retirement plans

Job summary

Myana in Philadelphia seeks a Senior Clinical Research Coordinator for Neurology. You'll oversee clinical trials, ensuring adherence to regulations while managing patient data and recruitment. Candidates must have extensive clinical research experience, with opportunities for training and development offered.

Join a team committed to advancing treatments in neurology within a supportive work environment that values equal opportunity and diversity.

Qualifications

• 6 years of clinical research experience, or 2 years with a Bachelor's degree, or 1 year with a Master's degree.

Responsibilities

• Oversee day-to-day clinical trial activities in accordance with Good Clinical Practice.
• Manage clinical trials from startup through closeout.
• Coordinate patient screening and recruitment.

Skills

Clinical research experience

Good Clinical Practice (GCP)

Regulatory compliance

Data management

Patient recruitment

Education

High School Diploma or equivalent

Bachelor's degree

Master's degree

Job description

Job Details

Senior Clinical Research Coordinator for Neurology works on observational and interventional research, spanning industry sponsored and investigator initiated clinical trials of novel treatments in multiple Neurology divisions. This is a patient facing position with responsibility for subject identification, consenting, data collection and entry, lab sample processing, and maintenance of study documentation according to federal regulations and good clinical practice guidelines.

Job Description

• Oversees day-to-day clinical trial activities in accordance with Good Clinical Practice (GCP) guidelines.
• Independently manages or assists with clinical trials from startup through closeout.
• Coordinates protocol-related activities, including patient screening, recruitment, enrollment, and informed consent.
• Conducts feasibility assessments and study planning activities.
• Manages clinical trial data and biological specimens.
• Prepares for sponsor monitoring visits and audits.
• Prepares and maintains regulatory and Institutional Review Board (IRB) documentation.
• Ensures study procedures are conducted in compliance with protocol requirements and applicable regulations.
• Trains and supervises research staff on GCP and study-specific procedures.
• Assists with onboarding and training of new team members.
• Develops and revises workflows, training materials, SOPs, and guidance documents.
• Participates in departmental workgroups and process improvement initiatives.
• Prepares and submits materials to the IRB and other regulatory bodies in a timely manner.
• Maintains subject enrollment and tracking logs.
• Tracks study-related expenses and submits documentation for grant and study payments.
• Performs quality control reviews to ensure data integrity and regulatory compliance.
• Organizes and maintains study records and patient documentation.
• Designs and manages electronic data capture databases, when applicable.
• Provides clerical and technical support to ensure adherence to research protocols and data quality.

Minimum Qualifications

• High School Diploma or equivalent with 6 years of clinical research experience, OR
• Bachelor's degree with 2 years of clinical research experience, OR
• Master's degree with 1 year of clinical research experience.

Work Shift

Workday Day (United States of America)

Worker Sub Type

Regular

Employee Entity

Thomas Jefferson University

Primary Location Address

901 Walnut Street, Philadelphia, Pennsylvania, United States of America

Equal Employment Opportunity

Jefferson is committed to providing equal educational and employment opportunities for all persons without regard to age, race, color, religion, creed, sexual orientation, gender, gender identity, marital status, pregnancy, national origin, ancestry, citizenship, military status, veteran status, handicap or disability or any other protected group or status.

Benefits

Jefferson offers a comprehensive package of benefits for full‑time and part‑time colleagues, including medical (including prescription), supplemental insurance, dental, vision, life and AD&D insurance, short‑ and long‑term disability, flexible spending accounts, retirement plans, tuition assistance, as well as voluntary benefits, which provide colleagues with access to group rates on insurance and discounts. Colleagues have access to tuition discounts at Thomas Jefferson University after one year of full time service or two years of part time service. All colleagues, including those who work less than part‑time (including per diem colleagues, adjunct faculty, and Jeff Temps), have access to medical (including prescription) insurance.