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Clinical Research Associate II

Remote:

Full Remote

Experience:

Junior (1-2 years)

Work from:

India

Offer summary

Qualifications:

Bachelor's degree in a scientific discipline or equivalent work experience, 1-2 years of relevant monitoring experience, Proficient with MS Office Suite, Knowledgeable in clinical research operations and regulations.

Key responsabilities:

Conducts remote and on-site monitoring visits
Documents observations and facilitates action item resolution

Emmes Large http://www.emmes.com

1001 - 5000 Employees

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Job description

Overview

Job Posting Title

India Remote/Bangladesh

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either onsite at investigative sites or remotely to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP.

Responsibilities

Under supervision of the project CRA staff oversight lead (i.e. Clinical Study Manager, Lead CRA, Project Manager, etc.), independently schedules and conducts remote and on-site monitoring visits such as qualification/pre-study visits, site initiation visits, interim/routine monitoring visits, closeout visits, and for-cause visits.
As part of the site visits, independently conducts Informed Consent (ICF) review, source data verification/source document review, review for compliance with required reporting/tracking of adverse events and protocol deviations, investigator site file review, laboratory tour and specimen storage assessment, pharmacy/Investigational Product (IP)/Investigational Device (ID) storage location tour and storage condition assessment, IP/ID accountability, facilities tours, and other activities per the site monitoring plan under minimal direction from the project CRA staff oversight lead.
Documents observations and monitoring activities in a site visit report at the conclusion of the visit.
Facilitates and oversees Action Item resolution post visit.
Helps to ensure that clinical sites are conducting the study in compliance with protocol/clinical investigational plan, SOPs, ICH GCP, and other applicable regulations.
Provides training and retraining to site staff including protocol, GCP/GDP, and other training under direction from the project CRA staff oversight lead.
Identifies areas requiring follow-up and improvement at each clinical study site and reports findings to project CRA staff oversight lead.
Ensures all visits are conducted according to country regulations, ICH GCP, and company standard operating procedures
Serves as point of contact for study site personnel to answer questions and resolve studyrelated issues under the direction of the project CRA staff oversight lead. CORPORATE CONFIDENTIAL
May assist with the development and/or review of study-related materials including protocls informed consent forms, monitoring plan, monitoring documents, etc.
Prepares for and attends project team meetings and provides updates on project status and site-specific performance
Works collaboratively and effectively in a project team environment including internal and external colleagues to meet project objectives and timelines
Participates in Investigator Meetings or other client meetings as needed
Assists with filing and archiving of study documents
Assists in preparing sites for audits and may provide support and cooperation during audits/inspections (including translation to Auditor if needed)
May assist with coordination of clinical study supplies
May assist with submission of applications/notifications to Institutional Review Board (IRB)/Ethics Committee (EC)/Regulatory Authority
May assist with site recruitment oversight activities such as developing focused patient recruitment strategies and action plans.
Performs site management activities as required
Other duties as assigned

Qualifications

Bachelor’s degree (scientific discipline preferred) or equivalent work experience
At least 1-2 years of relevant monitoring experience (on-site and remote) Required Skills/Abilities
Proficient with MS Office Suite
Excellent computer and organizational skills
High level of attention to detail required
Ability to work on varying projects and exercise critical thinking
Self-starter who can work remotely and a team player who can work cross functionally with some oversight
Knowledgeable in clinical research operations, including interpretation and implementation of country regulations/ICH guidelines, as required per their role as a CRA
Excellent organizational, interpersonal, and communication skills (both oral and written)
Demonstrated problem-solving skills, self-motivated, and adaptable to a dynamic environment
Knowledgeable in prioritization, problem-solving, organization, critical thinking, decisionmaking, time management, and planning activities
Ability to collaborate with internal and external colleagues and work well in a team-oriented setting Required Job Behavior

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