Senior Research Clinical Coordinator, Endocrine

Boston Medical Center•Boston, MA

3d•Onsite

About The Position

The Sr. Research Clinical Coordinator conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, enters data into sponsor-specific electronic data capture forms, performs administrative tasks, assists in grant preparation, and participates with the research team in preparation of data and other reports. Will also assist with audits and quality. Must be able to work independently and make sound judgment with study protocols, data evaluation, and recruitment strategies. Prepares and presents data reports. This is a senior level role which requires strong analytical skills and conceptual thinking. Must be able to work independently, identify problems, and develop sound solutions. Expected to introduce innovations to the research study and design research protocols in conjunction with the Principal Investigator. This position coordinates the lab activities and is expected to be a liaison and strong resource to the department.

Requirements

BA or BS required
Requires 3-5 years of directly related, progressively responsible experience
Research experience with diabetes devices required
Ability to design, prepare, deliver and evaluate clinical programs
High level time management, organizational and verbal/written communication skills
Administrative skills to meet regulatory requirements
Ability to meet the requirements of the varying funding sources
Ability to prepare and monitor budgets
Knowledge of current and developing clinical research trends
Sound interpersonal skills and the ability to supervise others
Ability to work independently and display initiative to introduce innovations to research study
Ability to identify problems and develop sound solutions
Ability to resolve technical problems and interpret acceptability of data results
Keen knowledge of data management programs

Nice To Haves

Master's Degree Preferred

Responsibilities

Responsible for quality control
Reviews work of trainees
Develops study budgets
Coordinates lab activities
Plans, Designs, Performs Statistical Analysis
Designs research protocols in conjunction with PI
May Develop systems for QA/QC
Independently judges suitability for research subjects
Acts as a liaison between Research Admin and Unit
Files adverse events with IRB
Recommends protocol changes and may assist with writing protocols and manuscripts
Acts as a liaison with Human Resources
May assume grant management responsibilities for unit
May train, orient, educate and address the competency of the staff, interns and volunteers
Coordinates staffing and schedules and coordinates lab activities
Acts as a resource for the department

Benefits

Competitive pay
Tuition reimbursement and tuition remission programs
Highly subsidized medical, dental, and vision insurance options
Access a wealth of ongoing training and development opportunities that will not only enhance your skills but also expand your knowledge base especially for individuals pursuing careers in medicine or biomedical research
Engage in groundbreaking research projects that are driving the forefront of biomedical science
Flexible Spending Accounts
403(b) savings matches
paid time off
career advancement opportunities
resources to support employee and family well-being