Clinical Research Coordinator - GU Oncology - Dana Farber
Boston, MA
About the Job
- Job ID:
- 33917
- Location:
- 450 Brookline Ave, Boston, MA 02215
- Category:
- Clinical Research
- Employment Type:
- Full time
- Work Location:
- Onsite: Full time on Campus
Overview
The position is unique in that it will perform both Clinical Research Coordinator and Research Technician work within the clinical research program and support the bench research lab. This position will be responsible for the management of Genitourinary Oncologic patient samples integral with our development of an organoid biobank and to support of our translational research for key clinical trials. Accuracy and attention to detail is critical in recording both the intake of patient samples and their monitoring. This research technician will support the research activities of the Freedman Lab and the Gelb biobank. Supports the Gelb Center research team in the overall conduct of translational research. May assist with clinical data curation. This is an exciting opportunity to be a part of a research team focused on studying cancer genetics and epigenetics in prostate cancer.
In addition, the position will also perform Research Technician duties.
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.
Responsibilities
- Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities.
- Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries.
- Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis.
- Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations.
- Responsible for organizing and preparing for both internal and external auditing and study monitoring visits.
- Coordination and management of clinical trials, including communication with Sponsors and regulatory authorities.
- Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved.
- Interact with study participants as directed/required by the protocol and/or study team.
- May be responsible for tissue sample work.
- The individual will be an integral member of the laboratory and is expected to provide intellectual input and take part in lab meetings with other members of the lab.
- Will be a part of the laboratory and will perform numerous wet lab techniques. The individual is responsible for coordination and execution of lab-based procedures and analyses.
Qualifications
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are equally committed to diversifying our faculty and staff. Cancer knows no boundaries and when it comes to hiring the most dedicated and diverse professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.
- Bachelor's Degree required, with 0-1 years of related experience preferred. Experience working in a medical or scientific research setting or comparable technology orientated business environment preferred.
- Excellent organization and communications skills required. Strong interpersonal skills; ability to effectively interact with all levels of staff and externals contacts. Must be detail oriented and have the ability to follow-through. Ability to effectively manage time and prioritize workload. Must practice discretion and adhere to hospital confidentiality guidelines at all times. Must have computer skills including the use of Microsoft Office.
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other groups as protected by law.