Clinical Project Lead

Artech Information System LLC; Bridgewater (MA); On-site; USD 120,000 - 150,000; Full time

Job summary

A leading technology firm is seeking a Clinical Study Director in Bridgewater, Massachusetts. This role involves medical supervision and support for clinical trials and projects, ensuring high-quality execution and compliance with regulations. Candidates should be licensed Medical Doctors with experience in Phase 2/3 clinical research. Strong expertise in therapeutics, medical training, and communication is essential, alongside knowledge of ICH and GCP guidelines.

Qualifications

• Licensed Medical Doctor or an international graduate with ECFMG certification.
• 2-3 years of experience in Phase 2/3 Clinical Research in the pharmaceutical industry.

Responsibilities

• Provide medical supervision of clinical trials and related activities.
• Accountable for medical review and collaborate with Pharmacovigilance.
• Conduct feasibility for studies with the feasibility manager.

Skills

Clinical Research

Medical Expertise

Phase 2/3 Clinical Research

Fluent English

Education

Licensed United States Medical Doctor

Certified by ECFMG

Job description

At the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight 21st century listed technology companies in the world to cross $1bn in Net Profit, $6bn in Revenue and $15bn in Market Capitalization.

Job Description

• This role is key for medical supervision and medical management of clinical trials proposed or to be performed by the Clinical Science & Operations Platform (CSO) of Sanofi R&D.
• The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical activities (clinical part of CTD for registration, feasibility, …) performed by the CSO. The CSD will provide appropriate medical input and support for all these clinical activities.
• He/she will provide medical training and medical information to study team(s), Clinical Study Units (CSUs) and investigators. He/she will be deeply involved in the feasibility process.
• He/she will be accountable for medical review and will collaborate and interact with Pharmacovigilance to review safety data.
• He/she will interact with Medical Advisors in CRUs or Disease Units), a specialization in a medical area would be requested or at least appreciated.

SCOPE

All clinical studies related to projects in clinical development (excluding Clinical & Exploratory Pharmacology studies) and medical investigations (e.g. Registry, survey) for projects in development or for marketed drugs.

KEY INDIVIDUAL ACCOUNTABILITIES

• Medical reference and medical expertise for operational strategy within the CSO for study registries he/she is allocated to
• Medical consultant for projects to be proposed to the CSO
• Medical contact for interaction with physicians responsible for the project or the study at the customer level
• Support with his/her medical knowledge and background a study or a project from
• business negotiation with customers to final product delivery (e.g. study completion or
• Conduct the feasibility for study/project with the feasibility manager and other team members (especially Medical Advisors in CSUs)
• Prepare and/or organize and/or participate to Investigator's Meetings, Steering Committees, Data Monitoring Committee meetings (only 'open' part of the DMC meetings).
• Prepare and/or approve any documents related to the study and requiring a medical expertise (extended synopsis, protocol, medical training material for study monitoring team and for investigators)
• Provide medical training to study team, CSUs (Medical Advisors, monitoring) and investigators
• Develop interaction with Medical Advisors in CSUs for the best knowledge of the study, compound protocol
• Participate to Investigators meetings
• Provide medical answers to questions from Health Authorities, IRB/Ethics Committees, investigators, experts
• Participate to clinical trial team (and cluster if any) meetings
• Accountable for the medical review of data done by the clinical trial team, the case by case review of safety events reported to GPE and coding of events and drugs
• Provide appropriate medical input for patient recruitment and retention strategy
• Support the CSUs and affiliates to develop network of KOLs and experts and to select National Coordinators or members of Study Committees
• Prepare and provide key medical information to investigators and/experts in respect with communication policies (e.g. study results, DMC advice)

KEY SHARED ACCOUNTABILITIES

• Feasibility results with feasibility managers
• Project/Study deliverables with the Clinical Study Team
• Operational strategy with Project Leader(s)
• Get support from the Unit Management Office to get appropriate medical staff in CSUs and to determine appropriate study budget according to medical considerations
• Collaborate to Adjudication Committee Review including prior patients' data review as needed
• Ensure high quality execution from a medical perspective with support of all functions &
• Quality & Continuous Improvement group
• Ensure appropriate documentation and investigations of safety cases with Global
• Pharmacovigilance and Epidemiology (GPE).
• Ensure high quality of coding with coding officers

Basic Qualifications

• Licensed United States Medical Doctor or an International medical graduate who has certification by the Educational Commission for Foreign Medical Graduates (ECFMG).
• 2-3 or more years of Phase 2/3 Clinical Research / Drug Development experience in the pharmaceutical industry.

Preferred Qualifications

• Knowledge in ICH, GCP and local regulations
• Fluent in English (writing and speaking)
• Additional Clinical Research and/or Drug Development experience in other therapeutic areas, especially Immunology.