We're Looking for Great People

Employment opportunities may arise from time to time. Please check back for current vacancies.

We are a dedicated, hard-working and fast growing team, and we invite you to apply to join us! In addition to a competitive salary, full-time employees are offered Health Benefits, Paid Time Off, and more.

To explore employment opportunities with AHRM Inc. please contact us at (716) 881-8200, or send your CV to careers@ahrminc.com

AHRM Inc. is an EOE.

Current Openings At AHRM Inc.

Full-Time Clinical Research Monitor/Buffalo, NY Office

Job Description

Delivery of high quality data according to agreed timelines and budget, ensuring adherence to international and local regulations and SOP standards.
Demonstrate exceptional customer focus as evidenced by positive feedback from colleagues and external customers (Investigators).
Participate in the site nomination process; perform evaluation of site capability to deliver the contractually agreed to number of patients and high quality data then make recommendation for inclusion in the clinical trial.
Assume ambassadorial role to facilitate communication between sites and line functions to increase value proposition to investigators.
Facilitate preparation and collection of site level documents.
Execute site initiation and training activities.
Perform monitoring visits according to monitoring plan and author study monitoring reports.
Manage site drug supply management.
Resolve site level update of technical systems (EDC).
Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc).
Manage recruitment implementing appropriate contingency plans as needed.
Assure continual GCP, ICH and SOP compliance (Informed consent process, source data verification, AE and SAE reporting, IN, protocol, drug accountability etc.).
Resolve deviations to standard by remedial action and training.
Perform data query resolution process (both at Site and with Data Management).
Execute site closeout activities.
May act as local (or global) CRA Lead, as assigned.
May act as a mentor to new associates for purposes of field training, as assigned.

Skills:

Basic medical and business knowledge. Desired competency in clinical research or having demonstrated adequate level of proficiency within the CRA competency profile. Understands and can apply knowledge of clinical trial designs to trial execution. Knowledge and experience in international standards (GCP/ICH), international (FDA, EMEA) and local regulations. Expertise in communication, managing multiple priorities and computer literacy.

Education:

A degree in a scientific or health care discipline preferred.

Requirements:

Regional CRA - (ACEG or SOCRA) - Must have a four year degree. Desired competency in clinical research or having demonstrated adequate level of proficiency within the CRA competency profile. Will consider training experienced data manager or trial coordinator, who is willing/able to obtain CRA certification based on current credentials. Must be able to travel up to 45% of the time. Salary and benefit package. No relocation package. LOCAL APPLICANTS PREFERRED

AHRM is an EOE.

Clinical Research Coordinator

Grant/Scientific Writer

Clinical Research Associate

Client Testimonial

"Our company worked with Amy Hayward and her team on a Phase III global clinical trial. The particular study I am referring to had multiple end points requiring a tight turn around with several hospital based sites throughout the US and internationally.

I found them to be extremely organized, efficient and professional. The team, under Amy’s supervision did great work for us on this study and I was very pleased with the results.

We were able to achieve high obtainable rates in terms of data collection and management on our randomized patients as well as adhere successfully to the time frames and deadlines outlined in the protocol.

They were reliable in terms of communication and feedback, and were diligent about meeting all of their obligations under the contract.

I would recommend them based on the successful completion of all deliverables we expected of them in terms of this project."

Senior Clinical Trial Manager
Omnicare