Current jobs related to Senior Clinical Research Associate - Bridgewater - Everest Clinical Research
-
Senior Director, Business Development
3 weeks ago
Bridgewater, Massachusetts, United States Everest Clinical Research Full timeAbout the RoleWe are seeking a highly skilled and experienced Senior Director, Business Development to join our team at Everest Clinical Research. As a key member of our business development team, you will be responsible for driving business growth and identifying new opportunities for our organization.Key ResponsibilitiesSource new client and project...
-
Research Associate
3 months ago
Bridgewater Township, United States Joulé Full timeJob Title: Senior Research Associate Location: Bridgewater, NJ Hours /Schedule: 8:30am - 5:30pm Type: Contract Overview Leading Pharmaceutical Company in NJ is seeking a Research Scientist with at least 2 years of experience in performing in-vitro assays. If you want to contribute to groundbreaking work in neutrophil-mediated disease research,...
-
Senior Research Associate
3 months ago
Bridgewater, United States Redbock - an NES Fircroft company Full timeSr. Research Associate (12-Month Contract // Bridgewater, NJ)The candidate will work with a multidisciplinary team of scientists and be engaged in the discovery, early development, and testing of novel pharmaceutical products to treat rare diseases.RESPONSIBILITIESDevelop, troubleshoot and execute studies of new products in cell-based and other in vitro...
-
Business Development Director
3 weeks ago
Bridgewater, Massachusetts, United States Everest Clinical Research Full timeAbout the RoleWe are seeking a highly skilled and experienced Business Development Director to join our team at Everest Clinical Research. As a key member of our organization, you will be responsible for driving business growth and development through strategic partnerships and client relationships.Key ResponsibilitiesSource new business opportunities and...
-
Research Associate
4 weeks ago
Bridgewater, United States Redbock - an NES Fircroft company Full timeResearch Associate (6-Month Contract // Bridgewater, NJ)Summary:We are seeking a candidate to be part of a team focused on non-viral vehicle formulation and characterization in the drug formulation group. The candidate will work with a multidisciplinary team of scientists and be engaged in targeted non-viral formulation development and...
-
Clinical Research Specialist
3 weeks ago
Bridgewater, New Jersey, United States Insmed Full timeCompany OverviewInsmed is a global biopharmaceutical organization dedicated to improving the lives of patients affected by serious and rare diseases. Our employees are our greatest asset, and our actions are driven by a commitment to a patients-first approach. We strive to expand our team with skilled professionals from around the globe who are eager to...
-
Research Scientist
3 weeks ago
Bridgewater, New Jersey, United States Joulé Full timeJob Title:Senior Research AssociateLocation: NJ Hours /Schedule: 8:30am - 5:30pm Type: Contract Job Summary: Joulé is seeking a highly skilled Research Scientist to join our team in Bridgewater, NJ. As a Research Scientist, you will be responsible for investigating therapeutics for treating neutrophil-mediated diseases.Responsibilities:Work with a...
-
Sr. Research Associate
3 months ago
Bridgewater, United States Redbock - an NES Fircroft company Full timeSr. Research Associate (12-Month Contract // Bridgewater, NJ)The candidate will work with a multidisciplinary team of scientists and be engaged in the discovery, early development, and testing of novel pharmaceutical products to treat rare diseases.RESPONSIBILITIESDevelop, troubleshoot and execute studies of new products in cell-based and other in vitro...
-
Sr. Research Associate
3 months ago
Bridgewater, United States Redbock - an NES Fircroft company Full timeSr. Research AssociateThe candidate will work with a multidisciplinary team of scientists and be engaged in the discovery, early development, and testing of novel pharmaceutical products to treat rare diseases. RESPONSIBILITIES• Develop, troubleshoot and execute studies of new products in cell-based and other in vitro assays • Isolate and culture primary...
-
Sr. Research Associate
3 months ago
Bridgewater, United States Redbock - an NES Fircroft company Full timeSr. Research AssociateThe candidate will work with a multidisciplinary team of scientists and be engaged in the discovery, early development, and testing of novel pharmaceutical products to treat rare diseases. RESPONSIBILITIES• Develop, troubleshoot and execute studies of new products in cell-based and other in vitro assays • Isolate and culture primary...
-
Part Time Library Associate
3 weeks ago
Bridgewater, Massachusetts, United States Bridgewater State University Full timeJob SummaryWe are seeking a highly skilled and detail-oriented Part Time Library Associate to provide reference and research services to our students, faculty, and staff, as well as to community users. As a key member of our team, you will be responsible for instructing users on how to search our library's catalog, print resources, and electronic...
-
Bridgewater, United States Joulé Full timeJob Title: Research Associate Location: Bridgewater, NJ Hours/Schedule: M-F, 8 am – 5 pm Type: Temporary to Hire Pay: $30-$34/hour with Bachelor's Degree, $35-$37/hour with Master's Degree (Depending Upon Experience) Overview Job supports: Early Pharma Research Seeking a candidate to be part of a team focused on non-viral vehicle formulation and...
-
Bridgewater, United States Ingredion Full timeHave a passion for the biotechnology and being a driving force in our pursuit of advancing the boundaries of biotransformation? Ingredion is looking for a Senior Manager, Biotransformation to play a pivotal role in guiding the Biotransformation Platform and overseeing the team and its diverse activities. You will manage key development and commercialization...
-
Sr. Quality Control Analyst
1 month ago
Bridgewater, United States Clinical Resource Network (CRN) Full timeOur client is looking to fill the role of Sr. Quality Control Analyst. This opportunity will be onsite in the Somerset, NJ area.Responsibilities:In-process materials, raw materials, finished product, or stability sample analysisSupporting cell therapy products and associated assaysResponsible for analytical test review and internal audit supportPrepare...
-
Senior Service Associate II
7 days ago
Bridgewater, Massachusetts, United States UPS Full timeJob SummaryWe are seeking a highly skilled and motivated Senior Service Associate II to join our team at UPS. As a key member of our healthcare team, you will be responsible for ensuring the efficient and accurate processing of healthcare products, including receipt, storage, and shipping.Key ResponsibilitiesReceive and process healthcare products, including...
-
Clinical Research Scientist
1 week ago
Bridgewater, New Jersey, United States Insmed Incorporated Full timeJob SummaryWe are seeking a highly skilled Clinical Research Scientist to join our team at Insmed Incorporated. As a key member of our clinical development team, you will play a critical role in supporting the development and execution of clinical protocols.Key ResponsibilitiesCollaborate with cross-functional teams to develop and implement clinical study...
-
Bridgewater, New Jersey, United States Ingredion Incorporated (Corporate) Full timeSenior Business Analyst/Associate Product Manager at IngredionIngredion is seeking a proactive Senior Business Analyst/Associate Product Manager to become a vital part of their Digital Innovation team. This position focuses on enhancing and refining data management and AI/ML platforms to foster product advancement in the food and industrial ingredients...
-
Senior Data Governance Analyst
5 days ago
Bridgewater, New Jersey, United States Bausch & Lomb Full timeAbout the RoleBausch + Lomb, a leading global eye health company, is seeking a Senior Master Data Governance Analyst to join our team. As a key member of our data governance team, you will play a critical role in developing and implementing data governance strategies and processes to ensure high-quality master data across our organization.Key...
-
Senior Clinician
2 months ago
Bridgewater, United States Spectrum Health Systems Full timeSenior Clinician Bridgewater, MA 02324, USA Req #3394 Monday, August 5, 2024 *Offering a $6,000 bonus!* Location: Bridgewater, MA - MOUD (Medications for Opioid Use Disorder) program at the Old Colony Correctional Center Schedule: Monday - Friday, 8:00am-4:00pm Pay rate: $72,000/annually Benefits: Health, dental,...
-
Senior Clinician
2 months ago
Bridgewater, United States Spectrum Health Systems Full timeSenior ClinicianBridgewater, MA 02324, USA Req #3394Monday, August 5, 2024*Offering a $6,000 bonus!*Location: Bridgewater, MA - MOUD (Medications for Opioid Use Disorder) program at the Old Colony Correctional Center Schedule: Monday - Friday, 8:00am-4:00pmPay rate: $72,000/annuallyBenefits: Health, dental, vision insurance 401k with company contribution...
Senior Clinical Research Associate
4 months ago
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Little Falls (Greater New York City Area), New Jersey, USA, and Shanghai (Pudong Zhangjiang New District), China.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that's us...that's Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team asSenior Clinical Research Associates for coverage on the East Coast (Eastern time zone). The incumbents may be required to travel to other locations across the USA to support monitoring activities as necessary.
Key Accountabilities:
- Interact with personnel from study sponsors, investigational sites, vendors, and Everest functional groups to enable timely and high quality initiations and completions of clinical trials.
- Identify, evaluate and qualify investigators and investigational sites for participation in clinical trials.
- Compile documentation for qualification of clinical sites. Review that documentation to ensure that those clinical sites comply with ICH-GCP and relevant local regulations.
- Assist with preparation and submission of regulatory documents to responsible authorities and IRB/ECs.
- Establish, maintain, and archive files of essential documents from investigative sites and for inclusion in Trial Master Files. These files must be maintained in a fashion so that they are continuously available for audit and completion for archive.
- Contribute to the development of documents that facilitate or describe the management of the clinical trial. Examples of such documents include Monitoring Plans, Risk Management Plans, study guides or manuals, and information collection tools.
- Develop and review documentation of information provided to study subjects, including informed consent forms.
- Assist with the preparation and negotiation of contracts with vendors and investigational sites.
- Participate in and prepare presentations for clinical trial initiation meetings such as investigator meetings or site monitor/coordinator training sessions. Address questions/concerns relevant to Clinical Operations from the meeting participants. Train Clinical Research Associates and site personnel on study requirements and procedures.
- Perform on-site monitoring of clinical studies.
- Document monitoring activities through submission of monitoring reports to Clinical Operations management for review, and through correspondence and telephone contact with investigative sites.
- Responsible for site management. Communicate directly with sites to provide direction, to assess performance, and to propose interventions to enhance enrollment performance.
- Monitor and report progress/status of investigational sites.
- Assist with investigator payments.
- Provide timely and accurate reports of travel expenses.
- Assist in the preparation, planning, and presentation of bid defenses.
- Participate in the development and maintenance of, and adhere to departmental SOPs and guidelines.
- Prepare, maintain, and complete training on study-specific and (or) applicable sponsor SOPs.
- Support sites in their efforts to prepare for audits conducted either by sponsors or regulatory authorities.
- Plan and carry out professional development.
Qualifications and Experience:
- Bachelor's degree in a life science or related field of study.
- Five years field monitoring clinical trials.
- Thorough knowledge of GCPs.
- Thorough comprehension of medical terminology.
- Excellent command of verbal and written English.
- Ability to travel a maximum of 70% of working hours is required.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website atwww.ecrscorp.com
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)
