Senior Clinical Research Coordinator - Hematology/Oncology

Description

The Senior Clinical Research Coordinator (Senior CRC)

contributes to the overall operational management of clinical

research/trial/study activities from design, set up, conduct, through closeout.

The position has responsibility for the implementation of research activities

for one or more studies. The Senior CRC recognizes and performs necessary tasks

to manage projects and prioritizes work to meet necessary deadlines. They are

responsible for planning and organizing necessary tasks to ensure adherence to

the study protocol and applicable regulations, such as institutional policy and

procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical

Practice (GCP). The Senior CRC collaborates with the Principal Investigator

(PI), ancillary departments, central research infrastructure teams, sponsors,

institutions, and other entities as needed to support the administration of all

aspects of studies, including, but not limited to, compliant conduct, financial

management, and adequate personnel support.. Performance of duties and tasks

will vary based on the department operations, the type of study and scope of

service.

Salary Range: $93,927.51 – 151,099.73 Annually

Qualifications

Required

• Minimum of 4+ years of experience in a clinical research

setting.

• Interpersonal skills to

effectively communicate information in a timely, professional manner and

establish and maintain cooperative and effective working relationships with

students, staff, faculty, external collaborators and administration and to work as a member of a team .

• Ability to effectively

communicate and interact with patients in

a compassionate and kind manner.

• Ability to set

priorities and complete ongoing tasks

with competing deadlines , with frequent interruptions, to meet the

programmatic and department needs, while complying with applicable University

policies and federal and state regulations.

• Analytical skills to

assess clinical research protocols and regulatory requirements, define

problems, formulate logical solutions, develop alternative solutions, make

recommendations, and initiate corrective actions.

• Close attention

to detail to ensure accuracy in

a fast-paced, fluctuating workload environment.

• Organization skills to

create and maintain administrative and regulatory files effectively as well as

independently balance the various tasks to ensure deadlines are met.

• Demonstrated proficiency with Adobe

and Microsoft suite software, especially Excel , to perform daily tasks efficiently and accurately.

• A learning and

professional growth mentality so that new software tools, systems, and

processes can be adopted quickly and efficiently.

• Knowledge of and experience working

with a variety of local and external

IRBs , scientific review

and other research committees ,

national cooperative group sponsors, industry sponsors, federal and foundation

funding organizations, etc.

• Strong verbal and written

communication skills to effectively establish rapport, building

collaborative relationships, and communicate complex concepts and ideas in an

easy-to-understand manner.

• Ability to adapt to

changing job demands and priorities , remain flexible including working flexible hours to accommodate research

deadlines.

• Ability to handle confidential

information with judgement and discretion.

• High degree of concentration

and focus in a work environment

that contains distracting stimuli, competing deadlines, and work delegated by

more than one individual.

• Availability to work in more than one environment, travelling to various clinic sites ,

meetings, conferences, etc.

• Strong knowledge of and experience working with a variety

of local and external IRBs, scientific review and other research committees,

• Strong knowledge of clinical research concepts, policies

and procedures, and human safety protection regulations and laws.

• Ability to think creatively to develop solutions affecting

the full team.

• Experience with FDA processes and procedures.
• Sufficient experience and knowledge of clinical trials

budgeting processes to manage the preparation of clinical trials budgets

Preferred

• Bachelor’s Degree in related area and/or equivalent

combination of education and experience. Advanced degree.