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:
A strong communicator with meticulous attention to detail, a successful Medical Writer has solid writing and organizational skills. They are curious and motivated, and work well independently or as part of a team in high-pressure situations.
Qualifications and skills required:
- Extensive knowledge of English grammar with a familiarity with a standard style guide
- Ability to communicate scientific or medical information in a clear and concise manner
- Proficiency in Word, Excel, PowerPoint, email, and the Internet
- Familiarity with the principles of clinical research
- Ability to interpret and present clinical data and other complex information
- Minimum 4 years’ experience.
Write, Review and Edit Scientific Medical Writing
Medical Writers compile, write, and edit medical writing deliverable s covering all phases of clinical research for submission to regulatory agencies. Medical Writers help write studies for submissions to the FDA. Their writing is also used in publications or medical journals, or for internal company use. Some of the things they write include comprehensive clinical study reports, study protocols, annual reports, investigator brochures, risk/benefit analysis and integrated summaries from raw data.
Write, Review and Edit Marketing Medical Writing
Medical Writers also write scientific copy for a broader audience, including scientific liaisons, healthcare professionals, and pharmaceutical representatives. They prepare abstracts, scientific exhibits, posters and verbal presentations. They also develop and write pharmaceutical training materials, eLearning content, video scripts, magazine articles, and presentations to be used by a variety of audiences.
Meet Standards and Requirements
A key task of the Medical Writer is to be sure that all deliverable s are in accordance with regulations, standards, and guidelines. The regulatory documents that the Medical Writer prepares must meet ICH, GLPs, and GCPs guidelines, a writing style guide, and often a company or client template. The Medical Writer must understand the levels of evidence required to achieve regulatory, marketing and regulatory goals.
Stay Current with Medical Literature and Advancements
In order to be effective in their job, a Medical Writer must be aware of current industry practices and regulatory requirements that affect medical writing. They must keep abreast of current literature, emerging science, technological developments and medical trends. They write summaries and maintain files on informative medical and scientific journal articles.
Can work from home up to 50% AFTER 3 months on the job.
Study Coordinator /Research Assistant
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.
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)
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.
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.