Clinical Research Associate II

Davita Inc.; Boston (MA); Remote; USD 60,000 - 80,000; Full time

Job summary

A leading healthcare company specializing in clinical trials seeks a Clinical Research Associate II to coordinate and monitor oncology trials. The role involves regulatory oversight, communication with trial sites, and ensuring compliance with protocols, with mostly remote work and minimal travel required.

Qualifications

• Minimum of 1-2 years directly related work experience.
• Possess working knowledge of clinical research protocols.
• Ability to work independently with general supervision.

Responsibilities

• Track trial progress and communicate with participating sites.
• Verify documentation and conduct onsite and remote monitoring.
• Submit reports to FDA, IRB, and stakeholders.

Skills

Attention to details

Organizational skills

Problem-solving skills

Communication skills

Ability to work remotely

Initiative

Analytical skills

Education

Bachelor's degree

Job description

General Summary/Overview Statement:
The Program for the Coordination and Oversight of Research Protocols (PCORP) within the MGH Cancer Center Protocol Office specializes in the central coordination, monitoring and regulatory oversight of Investigator-initiated, multi-center clinical trials. PCORP is seeking Clinical Research Associate (CRA) candidates to assist with the coordination and monitoring of multiple oncology trials.
The multi-center CRA works under general supervision to maintain regulatory files and monitor data quality and data and protocol compliance across participating study sites. The CRA will be trained on the institutional and federal regulations governing clinical research. The position involves a high volume of regulatory document coordination and tracking and clinical data review. This position does not include any direct patient contact.

Principle Duties & Responsibilities:

The CRA will perform the following duties under general supervision by the Clinical Research Manager:

* Track the progress of the trial across all participating sites (e.g., accrual, biospecimen collection and transfer, reportable events, regulatory submissions)

* Correspond with participating sites to support trial activities as needed:

o Answer questions about eligibility, study procedures or data entry

o Prepare and distribute informational updates, including meeting minutes, missing data reports and safety reports

o Communicate essential trial information and documentation, including protocol amendments; request routine updates from sites to maintain current study status

o Facilitate database reviews and query resolution

* Present the Sponsor-Investigator study status reports related to trial progress and assigned tasks

* Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all inclusion/exclusion criteria

* Conduct onsite and remote monitoring visits and complete corresponding monitoring reports (Domestic travel required for onsite monitoring <25%)

o Perform source document verification and drug accountability

o Review study site regulatory binder and essential documents for completeness and accuracy

o Evaluate ongoing protocol and data compliance

o Issue, track and resolve queries

* Gather, track and organize essential regulatory documents from participating sites

* Facilitate and document Sponsor-Investigator review of safety reports, investigational drug brochure updates, study violations and adverse events

* Submits routine and expedited reports to the FDA, IRB, funding sponsor or other stakeholders.

Skills/Abilities/Competencies Required

* Careful attention to details

* Superior organizational and time management skills and ability to prioritize multiple tasks

* Problem-solving skills, including the ability to gather information, identify resources, and develop alternatives

* Excellent written and oral communication skills

* Able to work successfully in a fully remote environment

* Demonstrate initiative and accountability

* Ability and willingness to travel nationally.

The Clinical Research Associate II should also possess:

* Working knowledge of clinical research protocols

* Ability to work independently with general supervision

* Analytical skills and ability to identify and resolve problems and develop alternatives

* Excellent judgment and ability to interpret information and protocol requirements

LICENSES, CERTIFICATIONS, and/or REGISTRATIONS:

* None

EDUCATION:

* Bachelor's degree required

EXPERIENCE:

* A minimum of 1-2 years of directly related work experience will be considered for a Clinical Research Associate II position.

SUPERVISORY RESPONSIBILITY:

* A Clinical Research Associate II may assist with the training and orientation of new staff members

FISCAL RESPONSIBILITY:

* CRAs are responsible for conducting onsite monitoring visits in adherence to institutional travel policy and submitting expense documentation in a timely fashion.

WORKING CONDITIONS:

* Duties will mainly be performed in a remote setting; limited in-office presence anticipated. Applicants may work in all states with the following exceptions: WY, ND, Puerto Rico, and the U.S. Virgin Islands.

* Less than 25% domestic travel (1-2 field visits per month maximum)

* Does not include patient contact

Mass General Brigham Incorporated is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.