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ccrpsorg · 1 year

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Medical Research Jobs

Medical research jobs provide individuals with the opportunity to make significant contributions to the advancement of medicine and healthcare. These positions involve conducting clinical trials, laboratory research, and analyzing data in order to develop new treatments for diseases. Working in medical research requires a high level of scientific knowledge, analytical skills, and critical thinking. Professionals in this field often collaborate with other researchers from different disciplines to conduct studies that aim to improve patient care and treatment options. Medical researchers also work closely with doctors, nurses, and other healthcare professionals so they can share their findings and better understand patient needs. With such a wide range of responsibilities, medical researchers play an essential role in driving innovation in the medical industry. The advancement of modern medicine is dependent on the insights that these professionals provide through their investigations. As such, medical research jobs offer ambitious individuals the chance to make a meaningful contribution to humanity’s ever-evolving knowledge of health and well-being.

Clinical Research Associate (CRA): Designs and implements clinical trials according to established protocols. Monitors the progress of trials and reports results to principal investigators. Salary range from $50,000 to $90,000 per year. CRA Certification through CCRPS requires completion of a 8-week course on research principles and methodology plus two years of experience in clinical research related activities such as site monitoring or data management.

Clinical Research Coordinator: This position involves coordinating the clinical aspects of research studies, such as collecting and organizing data, tracking recruitment of study participants, managing patient information, and monitoring research protocols. Salary range: $43,000 to $55,000 per year. Get CRC Certification through CCRPS: Certified Clinical Research Professional (CCRP).

Clinical Trials Manager (CTM): A Clinical Trials Manager is responsible for overseeing the entire clinical trial process from start to finish. They ensure the compliance of all study protocols while managing timelines and budgets. Salary range: $70,000-$90,000 per year; Certification through CCRPS: Certified Clinical Trial Manager (CCTM).

Medical Research Lab Technician: Responsible for performing laboratory tests according to established protocols in order to aid in medical research projects. Salary range: $35,000 to $45,000 per year. Certification through CCRPS: Certified Laboratory Technician (CLT).

Bioinformatics Scientist: Utilizes computer technology and statistical analysis in order to analyze biological data derived from experiments in medical research labs. Salary range: $75,000 to $100,000 per year Certification through CCRPS: Certified Bioinformatics Scientist (CBS).

Medical Writer: Writes and edits materials for clinical trials and other medical research projects, including study protocols and reports for publication or regulatory submission purposes. Salary range: $60,000 to $80,000 per year Certification through CCRPS: Certified Medical Writer (CMW).

Regulatory Affairs Manager: Manages the regulatory affairs process by ensuring that medical products adhere to applicable regulations throughout their development and commercialization phases. Salary range: $95,000 to $125,000 per year Certification through CCRPS for Certified Regulatory Affairs Manager (CARM)

Regulatory Affairs Specialist: Develops regulatory strategies for the submission of clinical trial applications to regulatory agencies, monitors global regulations governing clinical trial design and implementation and tracks changes in legislation affecting the development process of drugs, biologics or medical devices; coordinates communication between sponsors, investigators and regulatory authorities; prepares high-quality documents such as study protocols and amendments for submissions to regulatory bodies; participates in meetings with regulatory agencies worldwide; performs literature searches related to drug development topics; assists with ongoing maintenance of regulatory files as required by regulations. Salary range from $55,000 to $100,000 per year depending on experience level. Pharmacovigilance Certification through CCRPS requires completion of a 8-week course on research principles and methodology plus five years minimum experience in pharmaceutical industry or related fields with emphasis on Regulatory Affairs functions.

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evoldir · 3 years

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Fwd: Job: NewJersey.HumanBiodiversity

Begin forwarded message: > From: [email protected] > Subject: Job: NewJersey.HumanBiodiversity > Date: 12 August 2021 at 07:37:22 BST > To: [email protected] > Reply-To: > > > > Scientist > > Coriell Institute for Medical Research is currently seeking an experienced > scientist to join the Biobanking team. The ideal candidate for this > role is a PhD with postdoctoral experience and experience in human > genetics/genomics research. Additional experience in project and resource > management is desirable but not mandatory. We are interested in meeting > potential candidates with proven ability to effectively collaborate > with scientists and other department leads to oversee biorepository > management activities. > > The successful candidate will support landmark collections housed at > Coriell, including the NIGMS Human Genetic Cell Repository and NHGRI > Sample Repository for Human Genetic Research. S/he will also support > cutting-edge stem cell and genomic technologies employed for research > and biobanking at Coriell. > > Under the direction of the Chief Biobanking Officer, the incumbent > for this role will be responsible for partnering with other members > of Coriell’s Biobanking team to oversee and sustain the efficiency > and productivity of daily repository operations. Key responsibilities > include but are not limited to the following: > > · supporting ongoing contract and grant-related requirements > > · supporting internal and external reporting requirements > > · contributing to scientific conference presentations and peer reviewed > publications > > · supporting biorepository recruitment and outreach activities > > · actively participating in Coriell strategic initiatives and research > activities > > · contributing to external funding opportunity applications > > · performing other duties as assigned > > If you are interested in applying for this opportunity, please email > a cover letter and resume to [email protected]. Please include a > detailed description of your relevant experience in human genetics and/or > genomics, along with an explanation of any project and resource management > know-how. Applicants are encouraged to highlight their background with > non-profit, medical, healthcare, academic, and/or scientific research > organization(s). > > Now in its 60th year, Coriell Institute for Medical Research is an > independent non-profit research center dedicated to the study of the > human genome. Expert staff and pioneering programs in the fields of > molecular and cellular biology, genetics, genomics and epigenomics, > and biobanking drive our mission. To learn more, visit www.coriell.org. > > Coriell is committed to a respectful and inclusive working > environment. All qualified applicants will receive consideration for > employment without regard to race, color, national origin, religion, > sex, pregnancy, familial status, sexual orientation, gender identity or > expression, age, disability, genetic information, veteran status and all > other protected categories under federal or applicable state law. This > policy applies to all terms and conditions of employment, including > recruiting, hiring, placement, promotion, termination, layoff, recall, > transfer, leaves of absence, compensation and training. > > > Laura Scheinfeldt > via IFTTT

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