Careers at ELS
- Would you like to join a young and growing company, where you can make an immediate impact?
- Does the opportunity to be associated with a truly global organization devoted to excellence sound challenging?
- Would you feel excited to work with a highly qualified and motivated team of doctors, managers, clinicians and advisors?
If you answered, "yes" to these questions, then Excel Life Sciences is the right place for you.
Excel Life Sciences offers a challenging work environment that promotes creativity, innovation and leadership.
Currently we have the following open positions:
Clinical Research Coordinator
Description
Responsible for collecting data at clinical trial sites and assisting investigators in all aspects of clinical trial execution including pre-trial, during the trial and post trial activities.
Our Clinical Research Coordinators are dedicated to ensuring the safety and welfare of research subjects and maintaining scientific integrity throughout the clinical trial.
Job Responsibilities
- Site & PI identification as per the specific needs of Client & Protocol
- Regulatory submission
- IRB submission
- Site set up
- Document collection
- Create source document template
- Prepare site for SIV
- Pre screening, in case of chronic disease trials
- Enroll & Follow Up
- Assist in the ICF process, screening & enrollment
- Coordinate subject follow up visits - prevent lost to follow up & missed visits
- Manage CTM accountability, distribution & logistics
- Coordinate Central Lab logistics & sample flow
- Coordinate Monitoring & Audit visits
- Subject reimbursements
- Safety - Coordinate SAE reporting on time
- TMF - Maintain and update the file
- Post trial Activities
- Training - Project Specific & ICH GCP
- CRC - Recruit & Train CRC
- Investigator Meet - Organize multicentric trial meetings
- Contracts - Coordinate with all parties
- Financials - Coordinate for all milestone payments
- Create and Maintain local PI / Facility database
Requirements
This position requires a graduate in a scientific-related field. Any experience in clinical research would be a plus. Knowledge of ICH, FDA, and GCP regulations and practices is also a plus. Strong working knowledge of guidelines, and systems for clinical trial management. Excellent interpersonal, verbal, and written communication skills. Attention to detail and strong organizational skills.
To express your interest in this position, please click here.
Description
Responsible for working with the Director of Clinical Operations and the Excel Life Sciences team to develop systems to implement and manage all clinical trials. This position will provide broad oversight for all clinical research from protocol development to staff education.
- Reviewing all new protocols to determine requirements for implementation and feasibility
- Periodically reviewing staffing resources in order to identify staffing needs
- Serving as resource for protocol development, initiation and implementation
- Leading a team of clinical research personnel
- Assigning work and providing performance evaluations
- Developing and maintaining efficient, organized, systematic methods of protocol implementation
- Developing and preparing resource materials for clinical research staff education
- Working with Director of Clinical Operations and finance team to develop clinical trial budgets
Requirements
MBBS or MD preferred. Must have at least 2 years relevant experience in Clinical Trials
To express your interest in this position, please click here.
Assistant Medical Director
Description
Responsible for managing a team of project managers and serving as a resource to the organization and to our network of principal investigators and other stakeholders.
Job Responsibilities
- Bridge between Operations / BD internally
- Externally, represent ELS with physician groups, Pharmaceutical companies, NGOs, IRBs, patient advocacy groups and other stakeholders
- Manage feasibility reports
- Provide operational inputs to proposals
- Investigator Relationships including investigator and site analysis, communications and investigator forums
- Closely work with IRBs/ NGOs, patient groups cancer, Allergy, heart Disease, Lipid disorders, etc.
- Develop and improve patient recruitment strategies.
- Collaborates with the in house patient recruitment
- Prepare macro level documents on disease prevalence/SOC on most common conditions relevant to clinical research
- Understand the protocol requirements
- Include relevant questions in the feasibility questionnaire for the CRCs
- Compiles feasibility reports in user friendly formats
- Direct Project Managers to identify appropriate investigators, assist in the completion of the operational aspects of proposals e.g., regulatory challenges, recruitment and retention challenges, etc.
- Bi-monthly Investigator News Letter on topics of relevance and current interest
- Identify local/regional/national physician meetings for ELS speaking opportunities and participation
- Conduct community out reach programs in collaboration with IRBs/physicians/ hospital administrations, etc., on benefits of medical research, and participation in clinical research in particular
Qualifications
- Excellent people management skills
- Physician with Board Certification in Internal Medicine currently in a Junior Faculty Position.
- Prior experience in clinical research will be extremely desirable
- Physician from the pharmaceutical industry- with 3-4 years experience as a Medical Advisor
- Experienced in speaking / organizing product related meetings for the physicians
- Go getter
- Self starter
- Ability to network
- Good writing skills
- Personally well organized, and good at time management
- Willing to travel 40-50%
Requirements
MD required. Must have at least 2 years relevant experience in the pharmaceutical industry or clinical research industry.
To express your interest in this position, please click here.
Director of Sales, West Coast
Description:
Excel Life Sciences is interested in expanding its successful business development operation with the addition of a seasoned sales executive. This individual will be directly responsible for growth and management of the ELS business on the West Coast of the United States. All applicants must have a minimum of 10 years sales experience with at least 3 years of proven sales experience in the drug development and clinical research industry. Experience in dealing with biopharmaceutical companies carrying out global clinical trials and placing trials in non-U.S. locations will be a great advantage. Individuals must have strong relevant industry contacts.
Job Responsibilites:
- Develop a comprehensive business plan for raising awareness about Excel Life Sciences and securing new clients, including
- Identifying sales targets and building a strong pipeline
- Establishing quarterly / annual sales goals, comparing performance against goals and taking corrective action
- Defining the actions, timelines and frequency of sales efforts and execute as per plan
- Contact biopharmaceutical companies on the west coast to introduce Excel Life Sciences trial management services in India to prospective buyers in the clinical operations group
- Perform at least 3 hours of cold calls per day and 2 hours of follow up calls
- Involves travel up to 40% of the time
- Identify and participate in regional conferences and professional meetings where prospective clients may be present
- Conduct presentations at 2 or more industry conferences annually
- Write 2 articles to appear in industry trade magazines and journals annually
To express your interest in this position, please click here.
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