Senior Clinical Trial Associate, Clinical Operations

2 weeks ago


Menlo Park, United States ReCode Therapeutics Full time

Who We Are:

ReCode Therapeutics is a clinical-stage genetic medicines company using precision delivery to power the next wave of mRNA and gene correction therapeutics. ReCode's proprietary Selective Organ Targeting (SORT) lipid nanoparticle (LNP) platform enables highly precise and targeted delivery of genetic medicines directly to the organs, tissues and cells implicated in disease, enabling improved efficacy and potency. ReCode's lead programs include RCT1100 for the treatment of primary ciliary dyskinesia caused by pathogenic mutations in the DNAI1 gene, and RCT2100 for the treatment of the 10-13% of cystic fibrosis patients who have Class I mutations in the CFTR gene and do not respond to currently approved CFTR modulators. RCT1100 and RCT2100 are inhaled disease-modifying mRNA-based therapies formulated using the SORT LNP delivery platform. ReCode is expanding its pipeline to develop potential therapies for other rare and common genetic diseases, including musculoskeletal, central nervous system, liver and infectious disease indications.

Summary of Position:

The Senior Clinical Trial Associate (Contract) will report to the Clinical Operations Program Lead. You are a team player that will execute US and global clinical operations strategy for ReCode's programs. You will be responsible for collaborating with our cross-functional teams to deliver on ReCode's mission of powering the next wave of genetic medicines. You will have experience in either rare diseases or genetic medicines such as mRNA, gene therapy or gene editing.

This is a contract position for 40 hours/week.

Responsibilities:

* Manage eTMF process end to end in partnership with functional groups and CROs
* Provide administrative support to the Clinical Operations Department.
* Serve as a primary point of contact for project-related communications, managing correspondence and associated documents, and coordinate updates to distribution lists for sites, CROs, and vendors.
* Develop and maintain various study trackers (e.g. Patient trackers and Form FDA 1572 tracker).
* Facilitate study team meetings (i.e. SET), including scheduling, preparing agendas and minutes, and maintaining archives.
* Coordinate and manage study communications, including newsletters and updates.
* Support study start-up activities, including assigning site numbers and reviewing regulatory packets.
* Manage access to systems for CROs, vendors, and team members.
* Maintain systems to monitor study metrics and overall study information.
* Attend necessary study, project, and departmental meetings.

Qualifications:

* BS/BA required
* 2-3+ years of Clinical Operations experience in the biotech/pharma industries
* Rare disease/orphan drug experience a plus
* Clinical Operations experience across all phases of development from Phase 1-3 with emphasis on early phase development
* Strong working knowledge of ICH/GCP guidelines and thorough knowledge of clinical monitoring procedures
* Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team
* Highly responsive and proactive team player
* Strong organizational skills and able to prioritize and manage multiple ongoing projects simultaneously
* Excellent oral and written communication skills
* Champion for change within a fast-growing company/department

Salary Range: *$65-$80/hr

* Please note that for remote positions, salary may be adjusted for cost of living

Benefits Offered for Full-Time Employees:

* No premium cost for employees - 100% subsidized by ReCode for full-time employees
* Company 401k contribution
* 15 days of company paid holidays, including a holiday shutdown (usually the last week of the year)
* Mental health support for employees & their families
* FSA available, including a lifestyle spending account subsidized by company
* Employee discounts at hotspots

ReCode Therapeutics (www.recodetx.com) offers a competitive compensation/benefits package with a friendly, collaborative culture that values employee engagement and ongoing career development.

ReCode Therapeutics is an Equal Opportunity Employer.



  • Menlo Park, California, United States ReCode Therapeutics Full time

    Who We Are:ReCode Therapeutics is a clinical-stage genetic medicines company using precision delivery to power the next wave of mRNA and gene correction therapeutics. ReCode's proprietary Selective Organ Targeting (SORT) lipid nanoparticle (LNP) platform enables highly precise and targeted delivery of genetic medicines directly to the organs, tissues and...


  • Menlo Park, United States BioSpace Full time

    Job DetailsWho We Are: ReCode Therapeutics is a clinical-stage genetic medicines company using precision delivery to power the next wave of mRNA and gene correction therapeutics. ReCode's proprietary Selective Organ Targeting (SORT) lipid nanoparticle (LNP) platform enables highly precise and targeted delivery of genetic medicines directly to the organs,...


  • Menlo Park, United States Meet Full time

    Senior Manager, Clinical Supply Chain Planning: Location: Menlo Park, CA (Hybrid, 3 days onsite) Responsibilities: As the Senior Manager, Clinical Supply Chain Planning, you will be responsible for overseeing the operational activities related to the management of clinical trial materials. Working closely with cross-functional teams, including Clinical...


  • Menlo Park, United States Meet Full time

    Senior Manager, Clinical Supply Chain Planning:Location: Menlo Park, CA (Hybrid, 3 days onsite)Responsibilities:As the Senior Manager, Clinical Supply Chain Planning, you will be responsible for overseeing the operational activities related to the management of clinical trial materials. Working closely with cross-functional teams, including Clinical...


  • Menlo Park, United States Meet Full time

    Senior Manager, Clinical Supply Chain Planning:Location: Menlo Park, CA (Hybrid, 3 days onsite)Responsibilities:As the Senior Manager, Clinical Supply Chain Planning, you will be responsible for overseeing the operational activities related to the management of clinical trial materials. Working closely with cross-functional teams, including Clinical...


  • Menlo Park, United States Meet Full time

    Senior Manager, Clinical Supply Chain Planning:Location: Menlo Park, CA (Hybrid, 3 days onsite)Responsibilities:As the Senior Manager, Clinical Supply Chain Planning, you will be responsible for overseeing the operational activities related to the management of clinical trial materials. Working closely with cross-functional teams, including Clinical...


  • Oak Park, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionClinical Research Coordinator IIIA CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To...


  • Menlo Park, United States Summit Therapeutics plc Full time

    Our Mission: To build a viable, long-lasting health care organization that assumes full responsibility for designing, developing, trial execution and enrollment, regulatory submission and approval, and successful commercialization of patient, physician, caregiver, and societal-friendly medicinal therapy* intended to: improve quality of life, increase...


  • Menlo Park, United States Summit Therapeutics Sub, Inc. Full time

    Job DescriptionJob DescriptionOur Mission: To build a viable, long-lasting health care organization that assumes full responsibility for designing, developing, trial execution and enrollment, regulatory submission and approval, and successful commercialization of patient, physician, caregiver, and societal-friendly medicinal therapy* intended to: improve...


  • Park Ridge, United States Advocate Aurora Health Full time

    Department: 80022 Research - Clinical Trials: Neuro Status: Part time Benefits Eligible: No Hours Per Week: 0 Schedule Details/Additional Information: Casual/Per Diem position for Neuro Metric rating of cognitive and functional measurements for Clinical Trials. Major Responsibilities: Test Administration and Scoring Documentation. Skill Development....


  • Menlo Park, United States Meet Full time

    Associate Director, Clinical Supply ChainLocation: Menlo Park, CA (Hybrid, 3 days onsite)Responsibilities:The Associate Director, Clinical Supply Chain will play a pivotal role in overseeing the strategic planning and execution of clinical supply chain operations. Reporting to the Director of Supply Chain, this position will involve managing end-to-end...


  • Menlo Park, United States Meet Full time

    Associate Director, Clinical Supply Chain Location: Menlo Park, CA (Hybrid, 3 days onsite) Responsibilities: The Associate Director, Clinical Supply Chain will play a pivotal role in overseeing the strategic planning and execution of clinical supply chain operations. Reporting to the Director of Supply Chain, this position will involve managing end-to-end...


  • Menlo Park, United States Meet Full time

    Associate Director, Clinical Supply ChainLocation: Menlo Park, CA (Hybrid, 3 days onsite)Responsibilities:The Associate Director, Clinical Supply Chain will play a pivotal role in overseeing the strategic planning and execution of clinical supply chain operations. Reporting to the Director of Supply Chain, this position will involve managing end-to-end...


  • Menlo Park, United States Meet Full time

    Associate Director, Clinical Supply ChainLocation: Menlo Park, CA (Hybrid, 3 days onsite)Responsibilities:The Associate Director, Clinical Supply Chain will play a pivotal role in overseeing the strategic planning and execution of clinical supply chain operations. Reporting to the Director of Supply Chain, this position will involve managing end-to-end...


  • Overland Park, United States Altasciences Full time

    Responsibilities of the Clinical Research Technician I include execution of tasks performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors is respected. Understand protocol...


  • Winter Park, United States SQRL Full time

    Opportunity to join the Patient Recruitment Team of one of the fast-growing clinical research companies within the Winter Park, FL area! Great full-time position for Pre-Med students or those wanting to break into the Clinical Research industry! HighlightsPlay a major role in helping patients get involved in cutting-edge clinical trials - a meaningful...


  • Winter Park, United States SQRL Full time

    Opportunity to join the Patient Recruitment Team of one of the fast-growing clinical research companies within the Winter Park, FL area! Great full-time position for Pre-Med students or those wanting to break into the Clinical Research industry! HighlightsPlay a major role in helping patients get involved in cutting-edge clinical trials - a meaningful...


  • Menlo Park, United States Summit Therapeutics Sub, Inc. Full time

    Job DescriptionJob DescriptionLocation: Menlo Park, CA, or Remote West Coast USOur Mission:To build a viable long-lasting health care organization that assumes full responsibility for designing, developing, trial enrollment, regulatory approval and commercializing patient, physician, caregiver, payor, and societal friendly medicinal therapy intended to...


  • Rego Park, United States psg Full time

    Req Number 20798 Job Description Job Description Provides guidance to team members to implement, coordinate, and evaluate all clinical Pharmacy services. Monitors and evaluates medication usage, collaborates with the medical staff, and establishes cr Clinical, Pharmacy, Specialist, Senior, Clinic, Staff, Healthcare, Staffing


  • Menlo Park, CA, United States BillionToOne, Inc. Full time

    Principal Bioinformatics Associate Position Type: Full Time Leading the development projects for bioinformatics-related software and pipelines; proposing, project managing, and delivering architecture-level changes to bioinformatics software and infrastructure. Requirements: Masters degree in bioinformatics, computer science, computational biology, data...