Help Us Make Clinical Research Better

We are always looking for great people with clinical research experience. We have many opportunities at our facility for growth, and we would love to add more knowledge to our team. If you are experienced in Clinical Research in any of the areas listed, please send in your resume. We are interested in FT, PT, or PRN employees. If you are fabulous and can bring something great to our company, we want to hear from you.

Current Positions Available:

Study Coordinator /Research Assistant

Job description

Responsible for assisting with the implementation of clinical trials and overseeing and maintaining patient care and study understanding/compliance. Also responsible for accurately documenting all information obtained throughout the clinical research process.
Qualifications
Must be a high school graduate or have a GED equivalency.
Must have some knowledge of medical terms.
Must be able to effectively communicate with patients.
Must be reliable and self-motivated.
US Citizen/VISA required
Able to accommodate flexible work schedule (preferred)

Responsibilities
Responsible for performing safety assessments (blood draw, vital signs, EKG, adverse events, etc.) or study/investigational product specific assessments according to protocol and/or principal investigator instruction.
Assists in developing, completing, and maintaining source documents.
Screens, consents, and performs study procedures, as designated by Clinical Trial Manager.
Administers or coordinates the administration of investigational medication and follows subjects through the study period, per protocol.
Conduct required assessments throughout the clinical trial assessment period.
Interact with patients in friendly and helpful manner on a daily basis.
Responsible for maintaining and completing Case Report Forms in agreement with the source documentation and in accordance with study protocol.
Accompanies sponsors representatives during site visits and follows up, as needed.
Accumulates all data and supplies for study closure.
Depending on experience/qualifications responsibilities may include: assembling and distributing food for patients, maintaining patient rooms, disposing of garbage, providing clean linen, and overseeing/monitoring patients between study assessments.

Registered Nurse (RN) *Sign-on Bonus*

Job description
Responsible for assisting with the implementation of clinical trials, serving as a liaison between the investigative site and the pharmaceutical company, and overseeing and maintaining patient care and study understanding. Also responsible for accurately documenting all information obtained throughout the clinical research process.

Qualifications
Must be a Registered Nurse with a current license in the state in which the employee will be working.
Must not have any disciplinary action on license history.
Must be capable of performing all clinical tasks relevant to licensure and/or training.
Must be able to effectively communicate with patients.
Must have good interpersonal skills, demonstrated through interactions with patients, JBR staff, Sponsor representatives, etc.

Responsibilities

Responsible for nursing care of study patients, according to protocol requirements and/or JBR standing orders.
Develops, completes and maintains source documents.
Screens, consents, and performs study procedures, as designated by Clinical Trial Manager.
Administers or coordinates the administration of investigational medication and follows subjects through the study period, per protocol.
Conduct required assessments throughout the clinical trial assessment period.
Responsible for maintaining and completing Case Report Forms in agreement with the source documentation and in accordance with study protocol.
Assures drug and clinical supply accountability for assigned trials.
Accompanies sponsors representatives during site visits and follows up, as needed.
Accumulates all data and supplies for study closure.
Performs procedures (i.e. vital signs, laboratory tests, etc.), as required by protocol and as allowed by level of licensure and/or training.

Director of Business Development

Job description
JBR manages clinical research studies for entities seeking to determine the efficacy of pharmaceutical
interventions designed to address medical issues that impact humans. The company, which has an excellent reputation in the field, is seeking a professional to implement JBR’s comprehensive business development plan focused on acquiring and in other ways venturing with other reputable organizations in the field. The Director of Business Development will work closely with key members of the JBR leadership team to identify, quality and subsequently acquire clinical research site management organizations across the US.                                                                                                                                                               
Duties and Responsibilities

Work with JBR’s business development consultants to continuously develop and improve the companies business development database
Prospect for acquisition opportunities

When qualified opportunities are identified, work with aquisition candidates, building relationships, determining acceptable purchase terms and consummating purchase agreements
Work with CFO and business development consultants to determine the market value of acquisition candidates; present and negotiate purchase offers
Represent JBR as appropriate via presentations and participation in events                                                                                                                                                                            
Assure that acquisition candidates meet key representatives of JBR and that they understand the vision and values of JBR and are a good fit for JBR
Establish and maintain contact with organizations and businesses that may be acquisition candidates in the future                                                                                                               

Desired Skills and Abilities

Strong people skills
Very well organized
Efficient
Ability to understand and analyze, along with JBR’s leaders, the financial history and performance of acquisition candidates
Tenacious
Can see the big picture while focusing on the detail
Very strong listening skills                                                                                                                                                                                                                                                                   Very strong oral and written communication skills                                                                                                                                                                                                                            Can work independently while being a key player as part of the JBR business development team                                                                                                                                         Experience in health care

Benefits

Health, Dental, Vision benefits are offered for full time positions after 30 days of employment. 401k benefits are offered after one year. PTO, Sick and Holiday pay offered after 90 days. We offer a $2 differential for night shifts. 

JOB APPLICATION FORM

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