About Us:

CenExel Clinical Research and its fully owned and operated Centers of Excellence (research sites) provide unparalleled medical and scientific support in the design and execution of clinical trials.

Each of our research sites specializes 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, Movement Disorders, 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 after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary: Entry level position that provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and CBH guidelines, regulations, and policies.

Essential Responsibilities and Duties:

• Creating and maintaining screen books and patient charts for all assigned studies
• Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts
• Maintaining inventory of study-specific supplies including lab kits, assessments, and participant-facing materials
• Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication
• Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection
• Communicating with study participants, caregivers, third party vendors, and laboratories as needed
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks
• Aiding Coordinators in the facilitation of study monitoring visits
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants
• 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:

• Interest in and knowledge of specific study indications
• Excellent computer skills
• Advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc)
• Skill in organization and record maintenance
• Skill in developing and maintaining effective working relationships with supervisors and co-workers
• Strong personal initiative
• Ability to complete paperwork with precision and attention to detail
• Ability to react calmly and effectively in emergency situations
• Ability to interpret, adapt and apply guidelines and procedures
• Ability to clearly communicate both orally and verbally

Working Conditions

1. Indoor, Clinic environment.
2. Essential physical requirements include sitting, typing, standing, and walking.
3. Lightly active position, occasional lifting of up to 20 pounds.
4. 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.