ABOUT US

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

JOB SUMMARY

Responsible for initiating and implementing study start up activities for the daily operational and administrative functions of clinical study operations with a focus on project and resource management. Ensures the implementation of policies and procedures of site and regulatory agencies are met or exceeded. This is a Full Time opportunity, Monday-Friday from 8am-5pm.

DUTIES AND RESPONSIBILITIES DESCRIPTION

Coordinates clinical trial start-up activities including the following:

o Ensures that assigned start-up activities are on track and in accordance with client and internal expectations.

o Inventory, log, and organize study materials received during study start up.

o Distribute study materials to delegated individuals while maintaining accountability for the transfer of supplies.

Collaborates with clinical staff to ensure that studies are conducted efficiently and are completed with the highest quality standards and outcomes.

Communicates with external vendors including contract research organizations, sponsors and monitors on behalf of clinical staff.

Review clinical study documentation in adherence to protocol, ensuring compliance.

Participates in for mal training of study staff prior to first subject screening.

Assumes other duties and responsibilities as assigned.

The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

EDUCATION/EXPERIENCE/SKILLS

Must be able to effectively communicate verbally and in writing.

Thorough understanding of clinical research terminology, good clinical practices, regulatory and ethical guidelines and regulations

One year of experience in clinical research.

Strong customer service and client relationship skills.

Excellent organization and time management skills with strong ability to prioritize and multi-task across competing demands.

Excellent verbal/written communication skills with evidence of effective collaboration across businesses and functions.

High-level computer skills.

WORKING CONDITIONS

Indoor, Clinic and Office environment.

Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting of up to 20 pounds.

Reporting to work, as scheduled, is essential.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Job Type: Full-time

Benefits:

• 401(k)
• Dental insurance
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Referral program
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Ability to Relocate:

• Decatur, GA 30030: Relocate before starting work (Required)

Work Location: In person