[Work From Home] Thermo Fisher Scientific Hiring in Clinical Research

Thermo Fisher Scientific Hiring: Assistant Clinical Research Associate (Remote)

About Company
Thermo Fisher Scientific’s mission is to make the world healthier, cleaner, and safer. Join our Clinical Research team, part of our global contract research organization (CRO), to contribute to impactful work on a global scale. Operating in 100+ countries, we conduct clinical trials and develop novel frameworks for clinical research.

Position Name:
Assistant Clinical Research Associate (Remote)

Organization:
Thermo Fisher Scientific

Qualification:
B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences

Experience:
0 – 2 Years / Freshers welcome

Salary:
25,000 – 35,000 /month

Location:
Work From Home

Job Summary:
As an Assistant Clinical Research Associate (CRA), you will perform remote activities on assigned projects in collaboration with the Remote CRA, On-Site CRA, and study Clinical Trial Manager (CTM). Your responsibilities include providing support for site preparedness, logistical assistance to the monitoring process, and aiding with site management and remote monitoring tasks in accordance with SOPs and regulatory guidelines. You may also be involved in limited site contact activities during various study phases.

Key Responsibilities:

Responsibility	Description
Study and Site Management	Complete tasks as defined in the task matrix for assigned studies.
Training	Document study-specific training completion and orient/train on CRG/study-specific systems.
Pre-Study Support	Provide in-house support during pre-study assessments and waivers.
Informed Consent Forms	Customize Site Informed Consent Forms (ICF) as needed.
EMR/EHR Checklist	Perform remote review and support data collection.
Document Collection	Verify document collection and submission status.
Patient-Facing Materials	Review and translate materials as needed.
Vendor Qualification Processes	Support site staff with vendor-related qualification processes.
System Access Coordination	Coordinate system access for relevant site staff.
Logistics for Investigator Meetings (IM)	Coordinate logistics for Investigator Meetings.
Vendor Trackers Maintenance	Support maintenance of vendor trackers.
Study/Site Supply Management	Coordinate study/site supply management.
Crucial Document Collection	Support collection, review, and updating of crucial documents.
Monitoring Tools Review	Support ongoing remote review of monitoring tools.
Site Payments	Assist with site payments processes.
Reconciliation Tasks	Perform reconciliation tasks on assigned trials.
Other Site Management Tasks	Perform other assigned site management tasks as directed.

Keys to Success:

Education and Experience:

• Bachelor’s degree or equivalent.
• 0 to 2 years of relevant experience.

Knowledge, Skills, and Abilities:

• Basic medical/therapeutic area knowledge.
• Understanding of medical terminology.
• Familiarity with ICH GCP and applicable regulations.
• Effective oral and written communication skills.
• Excellent interpersonal and customer service skills.
• Strong attention to detail and time management skills.
• Proven flexibility and adaptability.
• Ability to work independently or in a team.
• Critical thinking skills for problem-solving.
• Proficient in MS Office and digital literacy.
• Ability to extract pertinent information from various sources.
• Excellent English language and grammar skills.