Ich Q10 Jobs in Boston

Sr. Regulatory Writing Manager Remote 9month contract with potential extension. US Citizenship or Permanent Resident is required. Job Description In this vital role you will prepare and coordinate the preparation of regulatory submission documents that comply with global regulatory s More...

Horizon Controls Group is now hiring all levels of Automation Engineers to install new highly complex equipment including robotics into a pharmaceutical manufacturing environment. The successful candidate will be involved in the designing implementing and validating automation systems More...

Title: Senior Clinical Study Lead Basking Ridge NJ Location This is urgent and will fill the role by May 6th since it is maternity leave placement The Temp Senior Clinical Study Lead (CSL) Clinical Experimental Sciences Operations (CES Ops) is accountable for the execution o More...

Job Title: Registered Dietitian/Nutrition Scientist Location: Columbus, OH - On-site Contract Duration: 3-month assignment Work Hours: Monday to Friday, 8:30 AM to 5:00 PM RD Dietitian/Nutrition Scientist - Pediatrics Nutrition Science Our location in Columbus, OH, currently More...

Job Title: - Case Management Assistant Job Location: - 3330 Lomita Boulevard Torrance, CA 90505 Job Duration: 3+ months (High Possibility of Extension) Pay Rate: $28.00/hour on W2 Shift: Day 5x8-Hour (08:00 - 16:30) Schedule is 5x8 with one weekend day Job Description: Required Qualif More...

Responsibilities: Education : BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience Participate in the development of the CMC regulatory strategy for post-approval small m More...

Responsibilities: Serves as functional lead, providing support and sharing technical expertise with other functions, especially the clinical/research scientists engaged in the scientific aspects of the clinical development study/project(s). Serves as lead study programmer on one or m More...

Description: 3rd shift role - 10pm - 8am Could be any of the following shift but will be set once they start working 3rd shift. MUST train on 1st for the first couple weeks. Sun-Wed, Mon-Thurs, Tues-Fri, or Wed - Sat - flexible to work OT on weekends 1. Can it extend - Yes 2. Is th More...

Responsibilities: Responsible to communicate new regulatory guidelines. Lead the strategic efforts in the interpretation of relevant and new quality guidelines to ensure that the current and phase appropriate requirements and standards are properly and timely implemented Provide su More...

Responsibilities: Support strategic initiatives by leading projects to design and deploy process and technology related improvements and monitoring of R&D vendor issues for trends across the operational areas Develop and write vendor issue procedures Support in developing establish More...

Responsibilities: Represent the Quality function on product and process development project teams. Actively support and engage in design reviews. Lead or support design activities including design verification, validation, specification setting and justification, test method develo More...

Position: Pricing and Contract Strategy Manager/Study Contract Manager (SCM) Location: Wilmington DE HYBRID (3 days onsite/2 days remote) Duration: Long Term Description: Study Contract Manager (SCM) play an important role in driving the costings and contracts being responsible for More...

Wilmington, DE Contract Duration: 10-36 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Specialist Study Management in the Wilmington, DE area. Must be local to Wilmington, DE, non-remote position Own and maintain quality for the study file as the loc More...

Wilmington, DE Contract Duration: 12-36 months Possibility for FTE Conversion Rate: Negotiable Responsibilities: Excellent employment opportunity for a Pricing and Contract Strategy Manager in the Wilmington, DE area. Local to Wilmington: HYBRID (3 days onsite/2 days remote) Study More...

Description: LOCATION: Local to Wilmington: HYBRID (3 days onsite/2 days remote) *Possibility for FTE Conversion* Study Contract Manager (SCM) play an important role in driving the costings and contracts being responsible for negotiation and budgeting in clinical trials and for dev More...

Responsibilities: Provide data management expertise and support to internal project teams, clients, and Clinical Research Organizations (CROs) Plan, perform and oversee development of specifications for eCRFs/CRF, edit checks, electronic data handling, manual review, and execution o More...

Description: Must meet all requirements for Clinical Research Associate position and have demonstrated proficiency in all relevant areas. With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required. Assures More...

Santa Monica, CA Contract Duration: 5-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Clinical Trials Management Associate II in the Santa Monica, CA area. (onsite) Must meet all requirements for Clinical Research Associate position and have de More...

Director, Clinical OperationsContract to PermProvide leadership and manage end-to-end processes involved in outsourced clinical trials, key deliverables are:Maintaining and remediation of operational efficiency at RT and designated CRO demonstrated by meeting development program goal More...

Sr. Manager / Associate Director Clinical Development Operations Remote but preference is East CoastReport to:Sr. Vice President, Clinical Development Operations (CDO) About Company Company (RTX) is a clinical-phase company. Our core technology combines proprietary dry-powder inhale More...

Responsibilities: Hands-on experience on validation of enterprise GxP applications systems such as BMRAM. Hands-on experience on validation and qualification of cloud-based applications. Experience on drafting and reviewing Validation Plan, Test Plan , Summary Reports and Traceabil More...

Responsibilities: Manage and prepare IND, NDA, BLA, and DMF regulatory applications in eCTD format for submission to the applicable regulatory authority (FDA/HC) in compliance with required timelines and specifications. Perform quality control procedures to ensure completion, correct More...

Responsibilities: Contribute to GRAIL's clinical programs such as MSK and STRIVE studies from a clinical data management perspective. Work closely with GRAIL study team members and strategic partners to ensure that clinical data captured is complete, consistent, and accurate. Perform More...